Canonical Allele Identifier: CA400177592
Gene: SGCA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50167666G>T , CM000679.2:g.50167666G>T GRCh38
NC_000017.10:g.48245027G>T , CM000679.1:g.48245027G>T GRCh37
NC_000017.9:g.45600026G>T NCBI36
NG_008889.1:g.6662G>T , LRG_203:g.6662G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000504073.2:c.242G>T ENSP00000422030.2:p.Arg81Leu
ENST00000511303.6:n.38-281G>T
ENST00000512526.2:c.242G>T ENSP00000426606.2:p.Arg81Leu
ENST00000682109.1:c.122G>T ENSP00000508041.1:p.Arg41Leu
ENST00000683294.1:c.242G>T ENSP00000508134.1:p.Arg81Leu
ENST00000262018.8:c.242G>T MANE Select ENSP00000262018.3:p.Arg81Leu
ENST00000262018.7:c.242G>T ENSP00000262018.3:p.Arg81Leu
ENST00000344627.10:c.242G>T ENSP00000345522.6:p.Arg81Leu
ENST00000502555.5:c.157+179G>T ENSP00000422817.1:n.157+179G>T
ENST00000511303.5:c.34-281G>T ENSP00000426104.1:n.34-281G>T
ENST00000512526.1:c.86G>T
ENST00000513821.5:c.242G>T ENSP00000426571.1:p.Arg81Leu
ENST00000513942.5:n.104-281G>T
ENST00000514934.1:c.*18+179G>T ENSP00000423168.1:n.*18+179G>T
NM_000023.2:c.242G>T , LRG_203t1:c.242G>T NP_000014.1:p.Arg81Leu
NM_001135697.1:c.242G>T NP_001129169.1:p.Arg81Leu
XM_011525120.1:c.242G>T XP_011523422.1:p.Arg81Leu
XM_011525121.1:c.242G>T XP_011523423.1:p.Arg81Leu
XM_011525122.1:c.242G>T XP_011523424.1:p.Arg81Leu
XM_011525123.1:c.242G>T XP_011523425.1:p.Arg81Leu
XM_011525124.1:c.6+179G>T XP_011523426.1:n.6+179G>T
XR_934517.1:n.308G>T
NM_000023.3:c.242G>T NP_000014.1:p.Arg81Leu
NM_001135697.2:c.242G>T NP_001129169.1:p.Arg81Leu
NR_135553.1:n.298G>T
XM_011525120.2:c.404G>T XP_011523422.2:p.Arg135Leu
XM_011525121.2:c.404G>T XP_011523423.2:p.Arg135Leu
XM_011525122.2:c.404G>T XP_011523424.2:p.Arg135Leu
XM_011525123.2:c.404G>T XP_011523425.2:p.Arg135Leu
XM_011525124.2:c.6+179G>T XP_011523426.1:n.6+179G>T
XM_024450873.1:c.6+179G>T XP_024306641.1:n.6+179G>T
XR_002958056.1:n.760G>T
NM_000023.4:c.242G>T MANE Select NP_000014.1:p.Arg81Leu
NM_001135697.3:c.242G>T NP_001129169.1:p.Arg81Leu
NR_135553.2:n.278G>T