Canonical Allele Identifier: CA400177466

Gene: SGCA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50167645G>C , CM000679.2:g.50167645G>C	GRCh38
NC_000017.10:g.48245006G>C , CM000679.1:g.48245006G>C	GRCh37
NC_000017.9:g.45600005G>C	NCBI36
NG_008889.1:g.6641G>C , LRG_203:g.6641G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000023.4:c.221G>C MANE Select	NP_000014.1:p.Arg74Pro
ENST00000262018.8:c.221G>C MANE Select	ENSP00000262018.3:p.Arg74Pro
NM_000023.2:c.221G>C , LRG_203t1:c.221G>C	NP_000014.1:p.Arg74Pro
NM_000023.3:c.221G>C	NP_000014.1:p.Arg74Pro
NM_001135697.1:c.221G>C	NP_001129169.1:p.Arg74Pro
NM_001135697.2:c.221G>C	NP_001129169.1:p.Arg74Pro
NM_001135697.3:c.221G>C	NP_001129169.1:p.Arg74Pro
NR_135553.1:n.277G>C
NR_135553.2:n.257G>C
ENST00000262018.7:c.221G>C	ENSP00000262018.3:p.Arg74Pro
ENST00000344627.10:c.221G>C	ENSP00000345522.6:p.Arg74Pro
ENST00000502555.5:c.157+158G>C	ENSP00000422817.1:n.157+158G>C
ENST00000504073.2:c.221G>C	ENSP00000422030.2:p.Arg74Pro
ENST00000511303.5:c.34-302G>C	ENSP00000426104.1:n.34-302G>C
ENST00000511303.6:n.38-302G>C
ENST00000512526.1:c.65G>C
ENST00000512526.2:c.221G>C	ENSP00000426606.2:p.Arg74Pro
ENST00000513821.5:c.221G>C	ENSP00000426571.1:p.Arg74Pro
ENST00000513942.5:n.104-302G>C
ENST00000514934.1:c.*18+158G>C	ENSP00000423168.1:n.*18+158G>C
ENST00000682109.1:c.101G>C	ENSP00000508041.1:p.Arg34Pro
ENST00000683294.1:c.221G>C	ENSP00000508134.1:p.Arg74Pro
XM_011525120.1:c.221G>C	XP_011523422.1:p.Arg74Pro
XM_011525120.2:c.383G>C	XP_011523422.2:p.Arg128Pro
XM_011525121.1:c.221G>C	XP_011523423.1:p.Arg74Pro
XM_011525121.2:c.383G>C	XP_011523423.2:p.Arg128Pro
XM_011525122.1:c.221G>C	XP_011523424.1:p.Arg74Pro
XM_011525122.2:c.383G>C	XP_011523424.2:p.Arg128Pro
XM_011525123.1:c.221G>C	XP_011523425.1:p.Arg74Pro
XM_011525123.2:c.383G>C	XP_011523425.2:p.Arg128Pro
XM_011525124.1:c.6+158G>C	XP_011523426.1:n.6+158G>C
XM_011525124.2:c.6+158G>C	XP_011523426.1:n.6+158G>C
XM_024450873.1:c.6+158G>C	XP_024306641.1:n.6+158G>C
XR_002958056.1:n.739G>C
XR_934517.1:n.287G>C