Canonical Allele Identifier: CA2263905378

Gene: SGCA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50167967C= , CM000679.2:g.50167967C=	GRCh38
NC_000017.10:g.48245328C= , CM000679.1:g.48245328C=	GRCh37
NC_000017.9:g.45600327C=	NCBI36
NG_008889.1:g.6963C= , LRG_203:g.6963C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504073.2:c.333C=	ENSP00000422030.2:p.Asp111=
ENST00000511303.6:n.58C=
ENST00000512526.2:c.324C=	ENSP00000426606.2:p.Asp108=
ENST00000682109.1:c.213C=	ENSP00000508041.1:p.Asp71=
ENST00000683226.1:n.43C=
ENST00000683294.1:c.333C=	ENSP00000508134.1:p.Asp111=
ENST00000262018.8:c.333C= MANE Select	ENSP00000262018.3:p.Asp111=
ENST00000262018.7:c.333C=	ENSP00000262018.3:p.Asp111=
ENST00000344627.10:c.333C=	ENSP00000345522.6:p.Asp111=
ENST00000502555.5:c.178C=	ENSP00000422817.1:p.Gln60=
ENST00000511303.5:c.54C=	ENSP00000426104.1:p.Asp18=
ENST00000512526.1:c.168C=
ENST00000513821.5:c.333C=	ENSP00000426571.1:p.Asp111=
ENST00000513942.5:n.124C=
ENST00000514934.1:c.*39C=	ENSP00000423168.1:n.*39C=
NM_000023.2:c.333C= , LRG_203t1:c.333C=	NP_000014.1:p.Asp111=
NM_001135697.1:c.333C=	NP_001129169.1:p.Asp111=
XM_011525120.1:c.333C=	XP_011523422.1:p.Asp111=
XM_011525121.1:c.333C=	XP_011523423.1:p.Asp111=
XM_011525122.1:c.333C=	XP_011523424.1:p.Asp111=
XM_011525123.1:c.333C=	XP_011523425.1:p.Asp111=
XM_011525124.1:c.27C=	XP_011523426.1:p.Asp9=
XR_934517.1:n.399C=
NM_000023.3:c.333C=	NP_000014.1:p.Asp111=
NM_001135697.2:c.333C=	NP_001129169.1:p.Asp111=
NR_135553.1:n.389C=
XM_011525120.2:c.495C=	XP_011523422.2:p.Asp165=
XM_011525121.2:c.495C=	XP_011523423.2:p.Asp165=
XM_011525122.2:c.495C=	XP_011523424.2:p.Asp165=
XM_011525123.2:c.495C=	XP_011523425.2:p.Asp165=
XM_011525124.2:c.27C=	XP_011523426.1:p.Asp9=
XM_024450873.1:c.27C=	XP_024306641.1:p.Asp9=
XR_002958056.1:n.851C=
NM_000023.4:c.333C= MANE Select	NP_000014.1:p.Asp111=
NM_001135697.3:c.333C=	NP_001129169.1:p.Asp111=
NR_135553.2:n.369C=