Canonical Allele Identifier: CA2263905625

Gene: SGCA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50168398A= , CM000679.2:g.50168398A=	GRCh38
NC_000017.10:g.48245759A= , CM000679.1:g.48245759A=	GRCh37
NC_000017.9:g.45600758A=	NCBI36
NG_008889.1:g.7394A= , LRG_203:g.7394A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504073.2:c.410A=	ENSP00000422030.2:p.Glu137=
ENST00000511303.6:n.135A=
ENST00000512526.2:c.401A=	ENSP00000426606.2:n.401A=
ENST00000682109.1:c.290A=	ENSP00000508041.1:p.Glu97=
ENST00000683226.1:n.120A=
ENST00000683294.1:c.410A=	ENSP00000508134.1:p.Glu137=
ENST00000262018.8:c.410A= MANE Select	ENSP00000262018.3:p.Glu137=
ENST00000262018.7:c.410A=	ENSP00000262018.3:p.Glu137=
ENST00000344627.10:c.410A=	ENSP00000345522.6:p.Glu137=
ENST00000502555.5:c.*69A=	ENSP00000422817.1:n.*69A=
ENST00000511303.5:c.131A=	ENSP00000426104.1:p.Glu44=
ENST00000512526.1:c.245A=
ENST00000513821.5:c.410A=	ENSP00000426571.1:p.Glu137=
ENST00000513942.5:n.201A=
ENST00000514934.1:c.*116A=	ENSP00000423168.1:n.*116A=
NM_000023.2:c.410A= , LRG_203t1:c.410A=	NP_000014.1:p.Glu137=
NM_001135697.1:c.410A=	NP_001129169.1:p.Glu137=
XM_011525120.1:c.410A=	XP_011523422.1:p.Glu137=
XM_011525121.1:c.410A=	XP_011523423.1:p.Glu137=
XM_011525122.1:c.410A=	XP_011523424.1:p.Glu137=
XM_011525123.1:c.410A=	XP_011523425.1:p.Glu137=
XM_011525124.1:c.104A=	XP_011523426.1:p.Glu35=
XR_934517.1:n.476A=
NM_000023.3:c.410A=	NP_000014.1:p.Glu137=
NM_001135697.2:c.410A=	NP_001129169.1:p.Glu137=
NR_135553.1:n.466A=
XM_011525120.2:c.572A=	XP_011523422.2:p.Glu191=
XM_011525121.2:c.572A=	XP_011523423.2:p.Glu191=
XM_011525122.2:c.572A=	XP_011523424.2:p.Glu191=
XM_011525123.2:c.572A=	XP_011523425.2:p.Glu191=
XM_011525124.2:c.104A=	XP_011523426.1:p.Glu35=
XM_024450873.1:c.104A=	XP_024306641.1:p.Glu35=
XR_002958056.1:n.928A=
NM_000023.4:c.410A= MANE Select	NP_000014.1:p.Glu137=
NM_001135697.3:c.410A=	NP_001129169.1:p.Glu137=
NR_135553.2:n.446A=