Canonical Allele Identifier: CA2263905630

Gene: SGCA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50168409C= , CM000679.2:g.50168409C=	GRCh38
NC_000017.10:g.48245770C= , CM000679.1:g.48245770C=	GRCh37
NC_000017.9:g.45600769C=	NCBI36
NG_008889.1:g.7405C= , LRG_203:g.7405C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504073.2:c.421C=	ENSP00000422030.2:p.Arg141=
ENST00000511303.6:n.146C=
ENST00000512526.2:c.412C=	ENSP00000426606.2:n.412C=
ENST00000682109.1:c.301C=	ENSP00000508041.1:p.Arg101=
ENST00000683226.1:n.131C=
ENST00000683294.1:c.421C=	ENSP00000508134.1:p.Arg141=
ENST00000262018.8:c.421C= MANE Select	ENSP00000262018.3:p.Arg141=
ENST00000262018.7:c.421C=	ENSP00000262018.3:p.Arg141=
ENST00000344627.10:c.421C=	ENSP00000345522.6:p.Arg141=
ENST00000502555.5:c.*80C=	ENSP00000422817.1:n.*80C=
ENST00000511303.5:c.142C=	ENSP00000426104.1:p.Arg48=
ENST00000512526.1:c.256C=
ENST00000513821.5:c.421C=	ENSP00000426571.1:p.Arg141=
ENST00000513942.5:n.212C=
ENST00000514934.1:c.*127C=	ENSP00000423168.1:n.*127C=
NM_000023.2:c.421C= , LRG_203t1:c.421C=	NP_000014.1:p.Arg141=
NM_001135697.1:c.421C=	NP_001129169.1:p.Arg141=
XM_011525120.1:c.421C=	XP_011523422.1:p.Arg141=
XM_011525121.1:c.421C=	XP_011523423.1:p.Arg141=
XM_011525122.1:c.421C=	XP_011523424.1:p.Arg141=
XM_011525123.1:c.421C=	XP_011523425.1:p.Arg141=
XM_011525124.1:c.115C=	XP_011523426.1:p.Arg39=
XR_934517.1:n.487C=
NM_000023.3:c.421C=	NP_000014.1:p.Arg141=
NM_001135697.2:c.421C=	NP_001129169.1:p.Arg141=
NR_135553.1:n.477C=
XM_011525120.2:c.583C=	XP_011523422.2:p.Arg195=
XM_011525121.2:c.583C=	XP_011523423.2:p.Arg195=
XM_011525122.2:c.583C=	XP_011523424.2:p.Arg195=
XM_011525123.2:c.583C=	XP_011523425.2:p.Arg195=
XM_011525124.2:c.115C=	XP_011523426.1:p.Arg39=
XM_024450873.1:c.115C=	XP_024306641.1:p.Arg39=
XR_002958056.1:n.939C=
NM_000023.4:c.421C= MANE Select	NP_000014.1:p.Arg141=
NM_001135697.3:c.421C=	NP_001129169.1:p.Arg141=
NR_135553.2:n.457C=