Canonical Allele Identifier: CA2263905414

Gene: SGCA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50168011A= , CM000679.2:g.50168011A=	GRCh38
NC_000017.10:g.48245372A= , CM000679.1:g.48245372A=	GRCh37
NC_000017.9:g.45600371A=	NCBI36
NG_008889.1:g.7007A= , LRG_203:g.7007A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504073.2:c.377A=	ENSP00000422030.2:p.Asp126=
ENST00000511303.6:n.102A=
ENST00000512526.2:c.368A=	ENSP00000426606.2:n.368A=
ENST00000682109.1:c.257A=	ENSP00000508041.1:p.Asp86=
ENST00000683226.1:n.87A=
ENST00000683294.1:c.377A=	ENSP00000508134.1:p.Asp126=
ENST00000262018.8:c.377A= MANE Select	ENSP00000262018.3:p.Asp126=
ENST00000262018.7:c.377A=	ENSP00000262018.3:p.Asp126=
ENST00000344627.10:c.377A=	ENSP00000345522.6:p.Asp126=
ENST00000502555.5:c.*36A=	ENSP00000422817.1:n.*36A=
ENST00000511303.5:c.98A=	ENSP00000426104.1:p.Asp33=
ENST00000512526.1:c.212A=
ENST00000513821.5:c.377A=	ENSP00000426571.1:p.Asp126=
ENST00000513942.5:n.168A=
ENST00000514934.1:c.*83A=	ENSP00000423168.1:n.*83A=
NM_000023.2:c.377A= , LRG_203t1:c.377A=	NP_000014.1:p.Asp126=
NM_001135697.1:c.377A=	NP_001129169.1:p.Asp126=
XM_011525120.1:c.377A=	XP_011523422.1:p.Asp126=
XM_011525121.1:c.377A=	XP_011523423.1:p.Asp126=
XM_011525122.1:c.377A=	XP_011523424.1:p.Asp126=
XM_011525123.1:c.377A=	XP_011523425.1:p.Asp126=
XM_011525124.1:c.71A=	XP_011523426.1:p.Asp24=
XR_934517.1:n.443A=
NM_000023.3:c.377A=	NP_000014.1:p.Asp126=
NM_001135697.2:c.377A=	NP_001129169.1:p.Asp126=
NR_135553.1:n.433A=
XM_011525120.2:c.539A=	XP_011523422.2:p.Asp180=
XM_011525121.2:c.539A=	XP_011523423.2:p.Asp180=
XM_011525122.2:c.539A=	XP_011523424.2:p.Asp180=
XM_011525123.2:c.539A=	XP_011523425.2:p.Asp180=
XM_011525124.2:c.71A=	XP_011523426.1:p.Asp24=
XM_024450873.1:c.71A=	XP_024306641.1:p.Asp24=
XR_002958056.1:n.895A=
NM_000023.4:c.377A= MANE Select	NP_000014.1:p.Asp126=
NM_001135697.3:c.377A=	NP_001129169.1:p.Asp126=
NR_135553.2:n.413A=