Canonical Allele Identifier: CA8643683
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 538663
dbSNP Id: rs573792379

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50167379G>A , CM000679.2:g.50167379G>A GRCh38
NC_000017.10:g.48244740G>A , CM000679.1:g.48244740G>A GRCh37
NC_000017.9:g.45599739G>A NCBI36
NG_008889.1:g.6375G>A , LRG_203:g.6375G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000504073.2:c.49G>A ENSP00000422030.2:p.Gly17Arg
ENST00000511303.6:n.38-568G>A
ENST00000512526.2:c.49G>A ENSP00000426606.2:p.Gly17Arg
ENST00000682109.1:c.38-203G>A ENSP00000508041.1:n.38-203G>A
ENST00000683294.1:c.49G>A ENSP00000508134.1:p.Gly17Arg
ENST00000262018.8:c.49G>A MANE Select ENSP00000262018.3:p.Gly17Arg
ENST00000262018.7:c.49G>A ENSP00000262018.3:p.Gly17Arg
ENST00000344627.10:c.49G>A ENSP00000345522.6:p.Gly17Arg
ENST00000502555.5:c.49G>A ENSP00000422817.1:p.Gly17Arg
ENST00000511303.5:c.34-568G>A ENSP00000426104.1:n.34-568G>A
ENST00000513821.5:c.49G>A ENSP00000426571.1:p.Gly17Arg
ENST00000513942.5:n.104-568G>A
ENST00000514934.1:c.108G>A ENSP00000423168.1:p.Gln36=
NM_000023.2:c.49G>A , LRG_203t1:c.49G>A NP_000014.1:p.Gly17Arg
NM_001135697.1:c.49G>A NP_001129169.1:p.Gly17Arg
XM_011525120.1:c.49G>A XP_011523422.1:p.Gly17Arg
XM_011525121.1:c.49G>A XP_011523423.1:p.Gly17Arg
XM_011525122.1:c.49G>A XP_011523424.1:p.Gly17Arg
XM_011525123.1:c.49G>A XP_011523425.1:p.Gly17Arg
XM_011525124.1:c.-103G>A XP_011523426.1:n.-103G>A
XR_934517.1:n.115G>A
NM_000023.3:c.49G>A NP_000014.1:p.Gly17Arg
NM_001135697.2:c.49G>A NP_001129169.1:p.Gly17Arg
NR_135553.1:n.105G>A
XM_011525120.2:c.211G>A XP_011523422.2:p.Gly71Arg
XM_011525121.2:c.211G>A XP_011523423.2:p.Gly71Arg
XM_011525122.2:c.211G>A XP_011523424.2:p.Gly71Arg
XM_011525123.2:c.211G>A XP_011523425.2:p.Gly71Arg
XM_011525124.2:c.-103G>A XP_011523426.1:n.-103G>A
XM_024450873.1:c.-103G>A XP_024306641.1:n.-103G>A
XR_002958056.1:n.567G>A
NM_000023.4:c.49G>A MANE Select NP_000014.1:p.Gly17Arg
NM_001135697.3:c.49G>A NP_001129169.1:p.Gly17Arg
NR_135553.2:n.85G>A