Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076473G>T , CM000676.2:g.65076473G>T	GRCh38
NC_000014.8:g.65543191G>T , CM000676.1:g.65543191G>T	GRCh37
NC_000014.7:g.64612944G>T	NCBI36
NG_029830.1:g.31037C>A , LRG_530:g.31037C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.*3C>A	ENSP00000452206.2:n.*3C>A
ENST00000556979.6:c.*939C>A	ENSP00000452378.1:n.*939C>A
ENST00000358664.9:c.*3C>A MANE Select	ENSP00000351490.4:n.*3C>A
ENST00000651648.1:c.145-6104C>A	ENSP00000498863.1:n.145-6104C>A
ENST00000284165.10:c.*1330C>A	ENSP00000284165.6:n.*1330C>A
ENST00000341653.6:c.171+17235C>A	ENSP00000342482.2:n.171+17235C>A
ENST00000358402.8:c.*3C>A	ENSP00000351175.4:n.*3C>A
ENST00000358664.8:c.*3C>A	ENSP00000351490.4:n.*3C>A
ENST00000394606.6:c.*259C>A	ENSP00000378104.2:n.*259C>A
ENST00000553928.5:c.*275C>A	ENSP00000451907.1:n.*275C>A
ENST00000555419.5:c.378C>A	ENSP00000452405.1:n.378C>A
ENST00000555932.5:c.227C>A	ENSP00000450763.1:p.Pro76Gln
ENST00000557277.5:c.*3C>A	ENSP00000450955.1:n.*3C>A
ENST00000618858.4:c.*275C>A	ENSP00000480127.1:n.*275C>A
NM_001271069.1:c.144+17235C>A	NP_001257998.1:n.144+17235C>A
NM_002382.4:c.*3C>A	NP_002373.3:n.*3C>A
NM_145112.2:c.*3C>A	NP_660087.1:n.*3C>A
NM_145113.2:c.*275C>A	NP_660088.1:n.*275C>A
NM_197957.3:c.171+17235C>A	NP_932061.1:n.171+17235C>A
NR_073137.1:n.610C>A
XR_429315.2:n.773C>A
NM_001320415.1:c.*3C>A	NP_001307344.1:n.*3C>A
XM_017021312.2:c.*3C>A	XP_016876801.1:n.*3C>A
XM_017021313.1:c.*3C>A	XP_016876802.1:n.*3C>A
XR_001750326.2:n.831C>A
XR_001750327.2:n.750C>A
XR_002957553.1:n.1264C>A
XR_943450.3:n.854C>A
XR_943451.3:n.870C>A
XR_943452.3:n.815C>A
NM_001320415.2:c.*3C>A	NP_001307344.1:n.*3C>A
NM_002382.5:c.*3C>A MANE Select	NP_002373.3:n.*3C>A
NM_145112.3:c.*3C>A	NP_660087.1:n.*3C>A
NM_145113.3:c.*275C>A	NP_660088.1:n.*275C>A
NM_001271069.2:c.144+17235C>A	NP_001257998.1:n.144+17235C>A
NM_197957.4:c.171+17235C>A	NP_932061.1:n.171+17235C>A

Linked Data

Genomic Alleles

Transcript Alleles