Canonical Allele Identifier: CA500828047

Gene: SGCA

Linked Data

• MyVariant Identifiers: chr17:g.48245082G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50167721G>A , CM000679.2:g.50167721G>A	GRCh38
NC_000017.10:g.48245082G>A , CM000679.1:g.48245082G>A	GRCh37
NC_000017.9:g.45600081G>A	NCBI36
NG_008889.1:g.6717G>A , LRG_203:g.6717G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504073.2:c.297G>A	ENSP00000422030.2:p.Gly99=
ENST00000511303.6:n.38-226G>A
ENST00000512526.2:c.297G>A	ENSP00000426606.2:p.Gly99=
ENST00000682109.1:c.177G>A	ENSP00000508041.1:p.Gly59=
ENST00000683226.1:n.7G>A
ENST00000683294.1:c.297G>A	ENSP00000508134.1:p.Gly99=
ENST00000262018.8:c.297G>A MANE Select	ENSP00000262018.3:p.Gly99=
ENST00000262018.7:c.297G>A	ENSP00000262018.3:p.Gly99=
ENST00000344627.10:c.297G>A	ENSP00000345522.6:p.Gly99=
ENST00000502555.5:c.158-226G>A	ENSP00000422817.1:n.158-226G>A
ENST00000511303.5:c.34-226G>A	ENSP00000426104.1:n.34-226G>A
ENST00000512526.1:c.141G>A
ENST00000513821.5:c.297G>A	ENSP00000426571.1:p.Gly99=
ENST00000513942.5:n.104-226G>A
ENST00000514934.1:c.*19-226G>A	ENSP00000423168.1:n.*19-226G>A
NM_000023.2:c.297G>A , LRG_203t1:c.297G>A	NP_000014.1:p.Gly99=
NM_001135697.1:c.297G>A	NP_001129169.1:p.Gly99=
XM_011525120.1:c.297G>A	XP_011523422.1:p.Gly99=
XM_011525121.1:c.297G>A	XP_011523423.1:p.Gly99=
XM_011525122.1:c.297G>A	XP_011523424.1:p.Gly99=
XM_011525123.1:c.297G>A	XP_011523425.1:p.Gly99=
XM_011525124.1:c.7-226G>A	XP_011523426.1:n.7-226G>A
XR_934517.1:n.363G>A
NM_000023.3:c.297G>A	NP_000014.1:p.Gly99=
NM_001135697.2:c.297G>A	NP_001129169.1:p.Gly99=
NR_135553.1:n.353G>A
XM_011525120.2:c.459G>A	XP_011523422.2:p.Gly153=
XM_011525121.2:c.459G>A	XP_011523423.2:p.Gly153=
XM_011525122.2:c.459G>A	XP_011523424.2:p.Gly153=
XM_011525123.2:c.459G>A	XP_011523425.2:p.Gly153=
XM_011525124.2:c.7-226G>A	XP_011523426.1:n.7-226G>A
XM_024450873.1:c.7-226G>A	XP_024306641.1:n.7-226G>A
XR_002958056.1:n.815G>A
NM_000023.4:c.297G>A MANE Select	NP_000014.1:p.Gly99=
NM_001135697.3:c.297G>A	NP_001129169.1:p.Gly99=
NR_135553.2:n.333G>A