Canonical Allele Identifier: CA400179864

Gene: SGCA

Linked Data

• gnomAD v4: 17-50168420-T-A
• MyVariant Identifiers: chr17:g.48245781T>A (hg19) ; chr17:g.50168420T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50168420T>A , CM000679.2:g.50168420T>A	GRCh38
NC_000017.10:g.48245781T>A , CM000679.1:g.48245781T>A	GRCh37
NC_000017.9:g.45600780T>A	NCBI36
NG_008889.1:g.7416T>A , LRG_203:g.7416T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000504073.2:c.432T>A	ENSP00000422030.2:p.Asp144Glu
ENST00000511303.6:n.157T>A
ENST00000512526.2:c.423T>A	ENSP00000426606.2:n.423T>A
ENST00000682109.1:c.312T>A	ENSP00000508041.1:p.Asp104Glu
ENST00000683226.1:n.142T>A
ENST00000683294.1:c.432T>A	ENSP00000508134.1:p.Asp144Glu
ENST00000262018.8:c.432T>A MANE Select	ENSP00000262018.3:p.Asp144Glu
ENST00000262018.7:c.432T>A	ENSP00000262018.3:p.Asp144Glu
ENST00000344627.10:c.432T>A	ENSP00000345522.6:p.Asp144Glu
ENST00000502555.5:c.*91T>A	ENSP00000422817.1:n.*91T>A
ENST00000511303.5:c.153T>A	ENSP00000426104.1:p.Asp51Glu
ENST00000512526.1:c.267T>A
ENST00000513821.5:c.432T>A	ENSP00000426571.1:p.Asp144Glu
ENST00000513942.5:n.223T>A
ENST00000514934.1:c.*138T>A	ENSP00000423168.1:n.*138T>A
NM_000023.2:c.432T>A , LRG_203t1:c.432T>A	NP_000014.1:p.Asp144Glu
NM_001135697.1:c.432T>A	NP_001129169.1:p.Asp144Glu
XM_011525120.1:c.432T>A	XP_011523422.1:p.Asp144Glu
XM_011525121.1:c.432T>A	XP_011523423.1:p.Asp144Glu
XM_011525122.1:c.432T>A	XP_011523424.1:p.Asp144Glu
XM_011525123.1:c.432T>A	XP_011523425.1:p.Asp144Glu
XM_011525124.1:c.126T>A	XP_011523426.1:p.Asp42Glu
XR_934517.1:n.498T>A
NM_000023.3:c.432T>A	NP_000014.1:p.Asp144Glu
NM_001135697.2:c.432T>A	NP_001129169.1:p.Asp144Glu
NR_135553.1:n.488T>A
XM_011525120.2:c.594T>A	XP_011523422.2:p.Asp198Glu
XM_011525121.2:c.594T>A	XP_011523423.2:p.Asp198Glu
XM_011525122.2:c.594T>A	XP_011523424.2:p.Asp198Glu
XM_011525123.2:c.594T>A	XP_011523425.2:p.Asp198Glu
XM_011525124.2:c.126T>A	XP_011523426.1:p.Asp42Glu
XM_024450873.1:c.126T>A	XP_024306641.1:p.Asp42Glu
XR_002958056.1:n.950T>A
NM_000023.4:c.432T>A MANE Select	NP_000014.1:p.Asp144Glu
NM_001135697.3:c.432T>A	NP_001129169.1:p.Asp144Glu
NR_135553.2:n.468T>A