Canonical Allele Identifier: CA400176450

Gene: SGCA

Linked Data

• ClinVar Variation Id: 2430699
• ClinVar RCV Id: RCV003129232
• dbSNP Id: rs760528436
• gnomAD v4: 17-50167398-C-A
• COSMIC: COSM385867
• MyVariant Identifiers: chr17:g.48244759C>A (hg19) ; chr17:g.50167398C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50167398C>A , CM000679.2:g.50167398C>A	GRCh38
NC_000017.10:g.48244759C>A , CM000679.1:g.48244759C>A	GRCh37
NC_000017.9:g.45599758C>A	NCBI36
NG_008889.1:g.6394C>A , LRG_203:g.6394C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504073.2:c.68C>A	ENSP00000422030.2:p.Ala23Asp
ENST00000511303.6:n.38-549C>A
ENST00000512526.2:c.68C>A	ENSP00000426606.2:p.Ala23Asp
ENST00000682109.1:c.38-184C>A	ENSP00000508041.1:n.38-184C>A
ENST00000683294.1:c.68C>A	ENSP00000508134.1:p.Ala23Asp
ENST00000262018.8:c.68C>A MANE Select	ENSP00000262018.3:p.Ala23Asp
ENST00000262018.7:c.68C>A	ENSP00000262018.3:p.Ala23Asp
ENST00000344627.10:c.68C>A	ENSP00000345522.6:p.Ala23Asp
ENST00000502555.5:c.68C>A	ENSP00000422817.1:p.Ala23Asp
ENST00000511303.5:c.34-549C>A	ENSP00000426104.1:n.34-549C>A
ENST00000513821.5:c.68C>A	ENSP00000426571.1:p.Ala23Asp
ENST00000513942.5:n.104-549C>A
ENST00000514934.1:c.127C>A	ENSP00000423168.1:p.Pro43Thr
NM_000023.2:c.68C>A , LRG_203t1:c.68C>A	NP_000014.1:p.Ala23Asp
NM_001135697.1:c.68C>A	NP_001129169.1:p.Ala23Asp
XM_011525120.1:c.68C>A	XP_011523422.1:p.Ala23Asp
XM_011525121.1:c.68C>A	XP_011523423.1:p.Ala23Asp
XM_011525122.1:c.68C>A	XP_011523424.1:p.Ala23Asp
XM_011525123.1:c.68C>A	XP_011523425.1:p.Ala23Asp
XM_011525124.1:c.-84C>A	XP_011523426.1:n.-84C>A
XR_934517.1:n.134C>A
NM_000023.3:c.68C>A	NP_000014.1:p.Ala23Asp
NM_001135697.2:c.68C>A	NP_001129169.1:p.Ala23Asp
NR_135553.1:n.124C>A
XM_011525120.2:c.230C>A	XP_011523422.2:p.Ala77Asp
XM_011525121.2:c.230C>A	XP_011523423.2:p.Ala77Asp
XM_011525122.2:c.230C>A	XP_011523424.2:p.Ala77Asp
XM_011525123.2:c.230C>A	XP_011523425.2:p.Ala77Asp
XM_011525124.2:c.-84C>A	XP_011523426.1:n.-84C>A
XM_024450873.1:c.-84C>A	XP_024306641.1:n.-84C>A
XR_002958056.1:n.586C>A
NM_000023.4:c.68C>A MANE Select	NP_000014.1:p.Ala23Asp
NM_001135697.3:c.68C>A	NP_001129169.1:p.Ala23Asp
NR_135553.2:n.104C>A