Canonical Allele Identifier: CA400180130

Gene: SGCA

Linked Data

• gnomAD v4: 17-50168557-A-T
• MyVariant Identifiers: chr17:g.48245918A>T (hg19) ; chr17:g.50168557A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50168557A>T , CM000679.2:g.50168557A>T	GRCh38
NC_000017.10:g.48245918A>T , CM000679.1:g.48245918A>T	GRCh37
NC_000017.9:g.45600917A>T	NCBI36
NG_008889.1:g.7553A>T , LRG_203:g.7553A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504073.2:c.569A>T	ENSP00000422030.2:p.Glu190Val
ENST00000511303.6:n.294A>T
ENST00000512526.2:c.560A>T	ENSP00000426606.2:n.560A>T
ENST00000682109.1:c.449A>T	ENSP00000508041.1:p.Glu150Val
ENST00000683226.1:n.279A>T
ENST00000683294.1:c.569A>T	ENSP00000508134.1:p.Glu190Val
ENST00000262018.8:c.569A>T MANE Select	ENSP00000262018.3:p.Glu190Val
ENST00000262018.7:c.569A>T	ENSP00000262018.3:p.Glu190Val
ENST00000344627.10:c.569A>T	ENSP00000345522.6:p.Glu190Val
ENST00000502555.5:c.*228A>T	ENSP00000422817.1:n.*228A>T
ENST00000504073.1:c.36A>T
ENST00000511303.5:c.290A>T	ENSP00000426104.1:p.Glu97Val
ENST00000512526.1:c.404A>T
ENST00000513821.5:c.569A>T	ENSP00000426571.1:p.Glu190Val
ENST00000513942.5:n.360A>T
ENST00000514934.1:c.*275A>T	ENSP00000423168.1:n.*275A>T
NM_000023.2:c.569A>T , LRG_203t1:c.569A>T	NP_000014.1:p.Glu190Val
NM_001135697.1:c.569A>T	NP_001129169.1:p.Glu190Val
XM_011525120.1:c.569A>T	XP_011523422.1:p.Glu190Val
XM_011525121.1:c.569A>T	XP_011523423.1:p.Glu190Val
XM_011525122.1:c.569A>T	XP_011523424.1:p.Glu190Val
XM_011525123.1:c.569A>T	XP_011523425.1:p.Glu190Val
XM_011525124.1:c.263A>T	XP_011523426.1:p.Glu88Val
XR_934517.1:n.635A>T
NM_000023.3:c.569A>T	NP_000014.1:p.Glu190Val
NM_001135697.2:c.569A>T	NP_001129169.1:p.Glu190Val
NR_135553.1:n.625A>T
XM_011525120.2:c.731A>T	XP_011523422.2:p.Glu244Val
XM_011525121.2:c.731A>T	XP_011523423.2:p.Glu244Val
XM_011525122.2:c.731A>T	XP_011523424.2:p.Glu244Val
XM_011525123.2:c.731A>T	XP_011523425.2:p.Glu244Val
XM_011525124.2:c.263A>T	XP_011523426.1:p.Glu88Val
XM_024450873.1:c.263A>T	XP_024306641.1:p.Glu88Val
XR_002958056.1:n.1087A>T
NM_000023.4:c.569A>T MANE Select	NP_000014.1:p.Glu190Val
NM_001135697.3:c.569A>T	NP_001129169.1:p.Glu190Val
NR_135553.2:n.605A>T