Canonical Allele Identifier: CA400177785

Gene: SGCA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50167695G>A , CM000679.2:g.50167695G>A	GRCh38
NC_000017.10:g.48245056G>A , CM000679.1:g.48245056G>A	GRCh37
NC_000017.9:g.45600055G>A	NCBI36
NG_008889.1:g.6691G>A , LRG_203:g.6691G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000023.4:c.271G>A MANE Select	NP_000014.1:p.Gly91Ser
ENST00000262018.8:c.271G>A MANE Select	ENSP00000262018.3:p.Gly91Ser
NM_000023.2:c.271G>A , LRG_203t1:c.271G>A	NP_000014.1:p.Gly91Ser
NM_000023.3:c.271G>A	NP_000014.1:p.Gly91Ser
NM_001135697.1:c.271G>A	NP_001129169.1:p.Gly91Ser
NM_001135697.2:c.271G>A	NP_001129169.1:p.Gly91Ser
NM_001135697.3:c.271G>A	NP_001129169.1:p.Gly91Ser
NR_135553.1:n.327G>A
NR_135553.2:n.307G>A
ENST00000262018.7:c.271G>A	ENSP00000262018.3:p.Gly91Ser
ENST00000344627.10:c.271G>A	ENSP00000345522.6:p.Gly91Ser
ENST00000502555.5:c.157+208G>A	ENSP00000422817.1:n.157+208G>A
ENST00000504073.2:c.271G>A	ENSP00000422030.2:p.Gly91Ser
ENST00000511303.5:c.34-252G>A	ENSP00000426104.1:n.34-252G>A
ENST00000511303.6:n.38-252G>A
ENST00000512526.1:c.115G>A
ENST00000512526.2:c.271G>A	ENSP00000426606.2:p.Gly91Ser
ENST00000513821.5:c.271G>A	ENSP00000426571.1:p.Gly91Ser
ENST00000513942.5:n.104-252G>A
ENST00000514934.1:c.*18+208G>A	ENSP00000423168.1:n.*18+208G>A
ENST00000682109.1:c.151G>A	ENSP00000508041.1:p.Gly51Ser
ENST00000683294.1:c.271G>A	ENSP00000508134.1:p.Gly91Ser
XM_011525120.1:c.271G>A	XP_011523422.1:p.Gly91Ser
XM_011525120.2:c.433G>A	XP_011523422.2:p.Gly145Ser
XM_011525121.1:c.271G>A	XP_011523423.1:p.Gly91Ser
XM_011525121.2:c.433G>A	XP_011523423.2:p.Gly145Ser
XM_011525122.1:c.271G>A	XP_011523424.1:p.Gly91Ser
XM_011525122.2:c.433G>A	XP_011523424.2:p.Gly145Ser
XM_011525123.1:c.271G>A	XP_011523425.1:p.Gly91Ser
XM_011525123.2:c.433G>A	XP_011523425.2:p.Gly145Ser
XM_011525124.1:c.6+208G>A	XP_011523426.1:n.6+208G>A
XM_011525124.2:c.6+208G>A	XP_011523426.1:n.6+208G>A
XM_024450873.1:c.6+208G>A	XP_024306641.1:n.6+208G>A
XR_002958056.1:n.789G>A
XR_934517.1:n.337G>A