Canonical Allele Identifier: CA2263906450

Gene: SGCA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50170067T= , CM000679.2:g.50170067T=	GRCh38
NC_000017.10:g.48247428T= , CM000679.1:g.48247428T=	GRCh37
NC_000017.9:g.45602427T=	NCBI36
NG_008889.1:g.9063T= , LRG_203:g.9063T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000504073.2:c.598-76T=	ENSP00000422030.2:n.598-76T=
ENST00000511303.6:n.310-573T=
ENST00000512526.2:c.576-573T=	ENSP00000426606.2:n.576-573T=
ENST00000682109.1:c.628-76T=	ENSP00000508041.1:n.628-76T=
ENST00000683226.1:n.1270T=
ENST00000683294.1:c.751T=	ENSP00000508134.1:p.Trp251=
ENST00000683544.1:n.38T=
ENST00000262018.8:c.748-76T= MANE Select	ENSP00000262018.3:n.748-76T=
ENST00000262018.7:c.748-76T=	ENSP00000262018.3:n.748-76T=
ENST00000344627.10:c.585-573T=	ENSP00000345522.6:n.585-573T=
ENST00000504073.1:c.65-76T=
ENST00000511303.5:c.306-573T=	ENSP00000426104.1:n.306-573T=
ENST00000512526.1:c.420-573T=
ENST00000513821.5:c.748-573T=	ENSP00000426571.1:n.748-573T=
ENST00000513942.5:n.376-573T=
NM_000023.2:c.748-76T= , LRG_203t1:c.748-76T=	NP_000014.1:n.748-76T=
NM_001135697.1:c.585-573T=	NP_001129169.1:n.585-573T=
XM_011525120.1:c.748-76T=	XP_011523422.1:n.748-76T=
XM_011525121.1:c.598-76T=	XP_011523423.1:n.598-76T=
XM_011525122.1:c.748-573T=	XP_011523424.1:n.748-573T=
XM_011525123.1:c.585-573T=	XP_011523425.1:n.585-573T=
XM_011525124.1:c.442-76T=	XP_011523426.1:n.442-76T=
XR_934517.1:n.814-573T=
NM_000023.3:c.748-76T=	NP_000014.1:n.748-76T=
NM_001135697.2:c.585-573T=	NP_001129169.1:n.585-573T=
NR_135553.1:n.804-573T=
XM_011525120.2:c.910-76T=	XP_011523422.2:n.910-76T=
XM_011525121.2:c.760-76T=	XP_011523423.2:n.760-76T=
XM_011525122.2:c.910-573T=	XP_011523424.2:n.910-573T=
XM_011525123.2:c.747-573T=	XP_011523425.2:n.747-573T=
XM_011525124.2:c.442-76T=	XP_011523426.1:n.442-76T=
XM_024450873.1:c.442-76T=	XP_024306641.1:n.442-76T=
XR_002958056.1:n.1269T=
NM_000023.4:c.748-76T= MANE Select	NP_000014.1:n.748-76T=
NM_001135697.3:c.585-573T=	NP_001129169.1:n.585-573T=
NR_135553.2:n.784-573T=