Canonical Allele Identifier: CA2263905645

Gene: SGCA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50168435G= , CM000679.2:g.50168435G=	GRCh38
NC_000017.10:g.48245796G= , CM000679.1:g.48245796G=	GRCh37
NC_000017.9:g.45600795G=	NCBI36
NG_008889.1:g.7431G= , LRG_203:g.7431G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504073.2:c.447G=	ENSP00000422030.2:p.Leu149=
ENST00000511303.6:n.172G=
ENST00000512526.2:c.438G=	ENSP00000426606.2:n.438G=
ENST00000682109.1:c.327G=	ENSP00000508041.1:p.Leu109=
ENST00000683226.1:n.157G=
ENST00000683294.1:c.447G=	ENSP00000508134.1:p.Leu149=
ENST00000262018.8:c.447G= MANE Select	ENSP00000262018.3:p.Leu149=
ENST00000262018.7:c.447G=	ENSP00000262018.3:p.Leu149=
ENST00000344627.10:c.447G=	ENSP00000345522.6:p.Leu149=
ENST00000502555.5:c.*106G=	ENSP00000422817.1:n.*106G=
ENST00000511303.5:c.168G=	ENSP00000426104.1:p.Leu56=
ENST00000512526.1:c.282G=
ENST00000513821.5:c.447G=	ENSP00000426571.1:p.Leu149=
ENST00000513942.5:n.238G=
ENST00000514934.1:c.*153G=	ENSP00000423168.1:n.*153G=
NM_000023.2:c.447G= , LRG_203t1:c.447G=	NP_000014.1:p.Leu149=
NM_001135697.1:c.447G=	NP_001129169.1:p.Leu149=
XM_011525120.1:c.447G=	XP_011523422.1:p.Leu149=
XM_011525121.1:c.447G=	XP_011523423.1:p.Leu149=
XM_011525122.1:c.447G=	XP_011523424.1:p.Leu149=
XM_011525123.1:c.447G=	XP_011523425.1:p.Leu149=
XM_011525124.1:c.141G=	XP_011523426.1:p.Leu47=
XR_934517.1:n.513G=
NM_000023.3:c.447G=	NP_000014.1:p.Leu149=
NM_001135697.2:c.447G=	NP_001129169.1:p.Leu149=
NR_135553.1:n.503G=
XM_011525120.2:c.609G=	XP_011523422.2:p.Leu203=
XM_011525121.2:c.609G=	XP_011523423.2:p.Leu203=
XM_011525122.2:c.609G=	XP_011523424.2:p.Leu203=
XM_011525123.2:c.609G=	XP_011523425.2:p.Leu203=
XM_011525124.2:c.141G=	XP_011523426.1:p.Leu47=
XM_024450873.1:c.141G=	XP_024306641.1:p.Leu47=
XR_002958056.1:n.965G=
NM_000023.4:c.447G= MANE Select	NP_000014.1:p.Leu149=
NM_001135697.3:c.447G=	NP_001129169.1:p.Leu149=
NR_135553.2:n.483G=