Canonical Allele Identifier: CA400180102

Gene: SGCA

Linked Data

• gnomAD v4: 17-50168542-T-A
• MyVariant Identifiers: chr17:g.48245903T>A (hg19) ; chr17:g.50168542T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50168542T>A , CM000679.2:g.50168542T>A	GRCh38
NC_000017.10:g.48245903T>A , CM000679.1:g.48245903T>A	GRCh37
NC_000017.9:g.45600902T>A	NCBI36
NG_008889.1:g.7538T>A , LRG_203:g.7538T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504073.2:c.554T>A	ENSP00000422030.2:p.Val185Asp
ENST00000511303.6:n.279T>A
ENST00000512526.2:c.545T>A	ENSP00000426606.2:n.545T>A
ENST00000682109.1:c.434T>A	ENSP00000508041.1:p.Val145Asp
ENST00000683226.1:n.264T>A
ENST00000683294.1:c.554T>A	ENSP00000508134.1:p.Val185Asp
ENST00000262018.8:c.554T>A MANE Select	ENSP00000262018.3:p.Val185Asp
ENST00000262018.7:c.554T>A	ENSP00000262018.3:p.Val185Asp
ENST00000344627.10:c.554T>A	ENSP00000345522.6:p.Val185Asp
ENST00000502555.5:c.*213T>A	ENSP00000422817.1:n.*213T>A
ENST00000504073.1:c.21T>A
ENST00000511303.5:c.275T>A	ENSP00000426104.1:p.Val92Asp
ENST00000512526.1:c.389T>A
ENST00000513821.5:c.554T>A	ENSP00000426571.1:p.Val185Asp
ENST00000513942.5:n.345T>A
ENST00000514934.1:c.*260T>A	ENSP00000423168.1:n.*260T>A
NM_000023.2:c.554T>A , LRG_203t1:c.554T>A	NP_000014.1:p.Val185Asp
NM_001135697.1:c.554T>A	NP_001129169.1:p.Val185Asp
XM_011525120.1:c.554T>A	XP_011523422.1:p.Val185Asp
XM_011525121.1:c.554T>A	XP_011523423.1:p.Val185Asp
XM_011525122.1:c.554T>A	XP_011523424.1:p.Val185Asp
XM_011525123.1:c.554T>A	XP_011523425.1:p.Val185Asp
XM_011525124.1:c.248T>A	XP_011523426.1:p.Val83Asp
XR_934517.1:n.620T>A
NM_000023.3:c.554T>A	NP_000014.1:p.Val185Asp
NM_001135697.2:c.554T>A	NP_001129169.1:p.Val185Asp
NR_135553.1:n.610T>A
XM_011525120.2:c.716T>A	XP_011523422.2:p.Val239Asp
XM_011525121.2:c.716T>A	XP_011523423.2:p.Val239Asp
XM_011525122.2:c.716T>A	XP_011523424.2:p.Val239Asp
XM_011525123.2:c.716T>A	XP_011523425.2:p.Val239Asp
XM_011525124.2:c.248T>A	XP_011523426.1:p.Val83Asp
XM_024450873.1:c.248T>A	XP_024306641.1:p.Val83Asp
XR_002958056.1:n.1072T>A
NM_000023.4:c.554T>A MANE Select	NP_000014.1:p.Val185Asp
NM_001135697.3:c.554T>A	NP_001129169.1:p.Val185Asp
NR_135553.2:n.590T>A