Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014676C>A , CM000672.2:g.89014676C>A	GRCh38
NC_000010.10:g.90774433C>A , CM000672.1:g.90774433C>A	GRCh37
NC_000010.9:g.90764413C>A	NCBI36
NG_009089.2:g.29146C>A , LRG_134:g.29146C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1543C>A
ENST00000355740.8:c.*557C>A	ENSP00000347979.3:n.*557C>A
ENST00000357339.7:c.*226C>A	ENSP00000349896.2:n.*226C>A
ENST00000371857.8:n.2779C>A
ENST00000460510.6:c.*226C>A	ENSP00000512812.1:n.*226C>A
ENST00000466081.6:n.2883C>A
ENST00000477270.6:c.*226C>A	ENSP00000512813.1:n.*226C>A
ENST00000492756.7:c.*663C>A	ENSP00000422453.1:n.*663C>A
ENST00000494799.6:c.*226C>A	ENSP00000512834.1:n.*226C>A
ENST00000562983.3:c.*226C>A	ENSP00000512845.1:n.*226C>A
ENST00000612663.6:c.*636C>A	ENSP00000477997.3:n.*636C>A
ENST00000640140.2:n.1379C>A
ENST00000640250.2:n.733C>A
ENST00000640681.2:n.1338C>A
ENST00000696723.1:n.4867C>A
ENST00000696741.1:n.2872C>A
ENST00000696742.1:n.2599C>A
ENST00000696743.1:n.4002C>A
ENST00000696744.1:n.1273C>A
ENST00000696767.1:n.1568C>A
ENST00000696768.1:c.*557C>A	ENSP00000512859.1:n.*557C>A
ENST00000696771.1:c.*226C>A	ENSP00000512860.1:n.*226C>A
ENST00000696772.1:n.2837C>A
ENST00000696773.1:n.2576C>A
ENST00000696774.1:n.6344C>A
ENST00000696776.1:c.*226C>A	ENSP00000512861.1:n.*226C>A
ENST00000696777.1:n.2642C>A
ENST00000696778.1:n.1670C>A
ENST00000696779.1:c.*226C>A	ENSP00000512862.1:n.*226C>A
ENST00000696780.1:c.*226C>A	ENSP00000512863.1:n.*226C>A
ENST00000696781.1:c.*226C>A	ENSP00000512864.1:n.*226C>A
ENST00000696782.1:c.*636C>A	ENSP00000512865.1:n.*636C>A
ENST00000696783.1:n.3102C>A
ENST00000696992.1:n.2351C>A
ENST00000696995.1:n.4763C>A
ENST00000696996.1:n.2676C>A
ENST00000696997.1:c.*864C>A	ENSP00000513028.1:n.*864C>A
ENST00000696998.1:n.2488C>A
ENST00000696999.1:c.*226C>A	ENSP00000513029.1:n.*226C>A
ENST00000697036.1:c.*650C>A	ENSP00000513060.1:n.*650C>A
ENST00000697037.1:n.1269C>A
ENST00000697093.1:n.3470C>A
ENST00000697094.1:n.3817C>A
ENST00000697095.1:c.*2435C>A	ENSP00000513104.1:n.*2435C>A
ENST00000697096.1:n.2367C>A
ENST00000697097.1:c.*226C>A	ENSP00000513105.1:n.*226C>A
ENST00000562983.2:n.1420C>A
ENST00000690268.1:c.*226C>A	ENSP00000509810.1:n.*226C>A
ENST00000355740.7:c.*560C>A	ENSP00000347979.3:n.*560C>A
ENST00000640140.1:n.1406C>A
ENST00000640250.1:n.733C>A
ENST00000640681.1:n.1355C>A
ENST00000652046.1:c.*226C>A MANE Select	ENSP00000498466.1:n.*226C>A
ENST00000352159.8:c.*551C>A	ENSP00000345601.4:n.*551C>A
ENST00000355740.6:c.*226C>A	ENSP00000347979.2:n.*226C>A
NM_000043.4:c.226C>A , LRG_134t1:c.226C>A	NP_000034.1:n.*226C>A
NM_152871.2:c.*226C>A	NP_690610.1:n.*226C>A
NM_152872.2:c.*546C>A	NP_690611.1:n.*546C>A
NR_028033.2:n.1408C>A
NR_028034.2:n.1270C>A
NR_028035.2:n.1333C>A
NR_028036.2:n.1471C>A
XM_006717819.2:c.*226C>A	XP_006717882.1:n.*226C>A
XM_011539764.1:c.*226C>A	XP_011538066.1:n.*226C>A
XM_011539765.1:c.*226C>A	XP_011538067.1:n.*226C>A
XM_011539766.1:c.*226C>A	XP_011538068.1:n.*226C>A
XM_011539767.1:c.*226C>A	XP_011538069.1:n.*226C>A
NM_000043.5:c.*226C>A	NP_000034.1:n.*226C>A
NM_001320619.1:c.*557C>A	NP_001307548.1:n.*557C>A
NM_152871.3:c.*226C>A	NP_690610.1:n.*226C>A
NM_152872.3:c.*546C>A	NP_690611.1:n.*546C>A
NR_028033.3:n.1380C>A
NR_028034.3:n.1242C>A
NR_028035.3:n.1305C>A
NR_028036.3:n.1443C>A
NR_135313.1:n.1360C>A
NR_135314.1:n.1543C>A
NR_135315.1:n.1296C>A
XM_006717819.3:c.*226C>A	XP_006717882.1:n.*226C>A
XM_011539764.2:c.*226C>A	XP_011538066.1:n.*226C>A
XM_011539765.2:c.*226C>A	XP_011538067.1:n.*226C>A
XM_011539766.2:c.*226C>A	XP_011538068.1:n.*226C>A
XM_011539767.3:c.*226C>A	XP_011538069.1:n.*226C>A
XR_945732.3:n.1302C>A
XR_945733.2:n.1239C>A
NM_000043.6:c.*226C>A MANE Select	NP_000034.1:n.*226C>A
NM_001320619.2:c.*557C>A	NP_001307548.1:n.*557C>A
NM_152871.4:c.*226C>A	NP_690610.1:n.*226C>A
NM_152872.4:c.*546C>A	NP_690611.1:n.*546C>A
NR_028033.4:n.1141C>A
NR_028034.4:n.1003C>A
NR_028035.4:n.1066C>A
NR_028036.4:n.1204C>A
NR_135313.2:n.1121C>A
NR_135314.2:n.1400C>A
NR_135315.2:n.1153C>A

Linked Data

Genomic Alleles

Transcript Alleles