Canonical Allele Identifier: CA2263905406

Gene: SGCA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50167996T= , CM000679.2:g.50167996T=	GRCh38
NC_000017.10:g.48245357T= , CM000679.1:g.48245357T=	GRCh37
NC_000017.9:g.45600356T=	NCBI36
NG_008889.1:g.6992T= , LRG_203:g.6992T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504073.2:c.362T=	ENSP00000422030.2:p.Val121=
ENST00000511303.6:n.87T=
ENST00000512526.2:c.353T=	ENSP00000426606.2:n.353T=
ENST00000682109.1:c.242T=	ENSP00000508041.1:p.Val81=
ENST00000683226.1:n.72T=
ENST00000683294.1:c.362T=	ENSP00000508134.1:p.Val121=
ENST00000262018.8:c.362T= MANE Select	ENSP00000262018.3:p.Val121=
ENST00000262018.7:c.362T=	ENSP00000262018.3:p.Val121=
ENST00000344627.10:c.362T=	ENSP00000345522.6:p.Val121=
ENST00000502555.5:c.*21T=	ENSP00000422817.1:n.*21T=
ENST00000511303.5:c.83T=	ENSP00000426104.1:p.Val28=
ENST00000512526.1:c.197T=
ENST00000513821.5:c.362T=	ENSP00000426571.1:p.Val121=
ENST00000513942.5:n.153T=
ENST00000514934.1:c.*68T=	ENSP00000423168.1:n.*68T=
NM_000023.2:c.362T= , LRG_203t1:c.362T=	NP_000014.1:p.Val121=
NM_001135697.1:c.362T=	NP_001129169.1:p.Val121=
XM_011525120.1:c.362T=	XP_011523422.1:p.Val121=
XM_011525121.1:c.362T=	XP_011523423.1:p.Val121=
XM_011525122.1:c.362T=	XP_011523424.1:p.Val121=
XM_011525123.1:c.362T=	XP_011523425.1:p.Val121=
XM_011525124.1:c.56T=	XP_011523426.1:p.Val19=
XR_934517.1:n.428T=
NM_000023.3:c.362T=	NP_000014.1:p.Val121=
NM_001135697.2:c.362T=	NP_001129169.1:p.Val121=
NR_135553.1:n.418T=
XM_011525120.2:c.524T=	XP_011523422.2:p.Val175=
XM_011525121.2:c.524T=	XP_011523423.2:p.Val175=
XM_011525122.2:c.524T=	XP_011523424.2:p.Val175=
XM_011525123.2:c.524T=	XP_011523425.2:p.Val175=
XM_011525124.2:c.56T=	XP_011523426.1:p.Val19=
XM_024450873.1:c.56T=	XP_024306641.1:p.Val19=
XR_002958056.1:n.880T=
NM_000023.4:c.362T= MANE Select	NP_000014.1:p.Val121=
NM_001135697.3:c.362T=	NP_001129169.1:p.Val121=
NR_135553.2:n.398T=