Canonical Allele Identifier: CA10605259

Gene: SGCA

Linked Data

• ClinVar Variation Id: 285818
• ClinVar RCV Id: RCV000403326 ; RCV000725732
• dbSNP Id: rs886043221
• gnomAD v4: 17-50168391-C-T
• MyVariant Identifiers: chr17:g.48245752C>T (hg19) ; chr17:g.50168391C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50168391C>T , CM000679.2:g.50168391C>T	GRCh38
NC_000017.10:g.48245752C>T , CM000679.1:g.48245752C>T	GRCh37
NC_000017.9:g.45600751C>T	NCBI36
NG_008889.1:g.7387C>T , LRG_203:g.7387C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504073.2:c.403C>T	ENSP00000422030.2:p.Gln135Ter
ENST00000511303.6:n.128C>T
ENST00000512526.2:c.394C>T	ENSP00000426606.2:n.394C>T
ENST00000682109.1:c.283C>T	ENSP00000508041.1:p.Gln95Ter
ENST00000683226.1:n.113C>T
ENST00000683294.1:c.403C>T	ENSP00000508134.1:p.Gln135Ter
ENST00000262018.8:c.403C>T MANE Select	ENSP00000262018.3:p.Gln135Ter
ENST00000262018.7:c.403C>T	ENSP00000262018.3:p.Gln135Ter
ENST00000344627.10:c.403C>T	ENSP00000345522.6:p.Gln135Ter
ENST00000502555.5:c.*62C>T	ENSP00000422817.1:n.*62C>T
ENST00000511303.5:c.124C>T	ENSP00000426104.1:p.Gln42Ter
ENST00000512526.1:c.238C>T
ENST00000513821.5:c.403C>T	ENSP00000426571.1:p.Gln135Ter
ENST00000513942.5:n.194C>T
ENST00000514934.1:c.*109C>T	ENSP00000423168.1:n.*109C>T
NM_000023.2:c.403C>T , LRG_203t1:c.403C>T	NP_000014.1:p.Gln135Ter
NM_001135697.1:c.403C>T	NP_001129169.1:p.Gln135Ter
XM_011525120.1:c.403C>T	XP_011523422.1:p.Gln135Ter
XM_011525121.1:c.403C>T	XP_011523423.1:p.Gln135Ter
XM_011525122.1:c.403C>T	XP_011523424.1:p.Gln135Ter
XM_011525123.1:c.403C>T	XP_011523425.1:p.Gln135Ter
XM_011525124.1:c.97C>T	XP_011523426.1:p.Gln33Ter
XR_934517.1:n.469C>T
NM_000023.3:c.403C>T	NP_000014.1:p.Gln135Ter
NM_001135697.2:c.403C>T	NP_001129169.1:p.Gln135Ter
NR_135553.1:n.459C>T
XM_011525120.2:c.565C>T	XP_011523422.2:p.Gln189Ter
XM_011525121.2:c.565C>T	XP_011523423.2:p.Gln189Ter
XM_011525122.2:c.565C>T	XP_011523424.2:p.Gln189Ter
XM_011525123.2:c.565C>T	XP_011523425.2:p.Gln189Ter
XM_011525124.2:c.97C>T	XP_011523426.1:p.Gln33Ter
XM_024450873.1:c.97C>T	XP_024306641.1:p.Gln33Ter
XR_002958056.1:n.921C>T
NM_000023.4:c.403C>T MANE Select	NP_000014.1:p.Gln135Ter
NM_001135697.3:c.403C>T	NP_001129169.1:p.Gln135Ter
NR_135553.2:n.439C>T