Canonical Allele Identifier: CA500828136

Gene: SGCA

Linked Data

• ClinVar Variation Id: 2038679
• ClinVar RCV Id: RCV002895136
• MyVariant Identifiers: chr17:g.48245337T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50167976T>C , CM000679.2:g.50167976T>C	GRCh38
NC_000017.10:g.48245337T>C , CM000679.1:g.48245337T>C	GRCh37
NC_000017.9:g.45600336T>C	NCBI36
NG_008889.1:g.6972T>C , LRG_203:g.6972T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504073.2:c.342T>C	ENSP00000422030.2:p.Asp114=
ENST00000511303.6:n.67T>C
ENST00000512526.2:c.333T>C	ENSP00000426606.2:n.333T>C
ENST00000682109.1:c.222T>C	ENSP00000508041.1:p.Asp74=
ENST00000683226.1:n.52T>C
ENST00000683294.1:c.342T>C	ENSP00000508134.1:p.Asp114=
ENST00000262018.8:c.342T>C MANE Select	ENSP00000262018.3:p.Asp114=
ENST00000262018.7:c.342T>C	ENSP00000262018.3:p.Asp114=
ENST00000344627.10:c.342T>C	ENSP00000345522.6:p.Asp114=
ENST00000502555.5:c.*1T>C	ENSP00000422817.1:n.*1T>C
ENST00000511303.5:c.63T>C	ENSP00000426104.1:p.Asp21=
ENST00000512526.1:c.177T>C
ENST00000513821.5:c.342T>C	ENSP00000426571.1:p.Asp114=
ENST00000513942.5:n.133T>C
ENST00000514934.1:c.*48T>C	ENSP00000423168.1:n.*48T>C
NM_000023.2:c.342T>C , LRG_203t1:c.342T>C	NP_000014.1:p.Asp114=
NM_001135697.1:c.342T>C	NP_001129169.1:p.Asp114=
XM_011525120.1:c.342T>C	XP_011523422.1:p.Asp114=
XM_011525121.1:c.342T>C	XP_011523423.1:p.Asp114=
XM_011525122.1:c.342T>C	XP_011523424.1:p.Asp114=
XM_011525123.1:c.342T>C	XP_011523425.1:p.Asp114=
XM_011525124.1:c.36T>C	XP_011523426.1:p.Asp12=
XR_934517.1:n.408T>C
NM_000023.3:c.342T>C	NP_000014.1:p.Asp114=
NM_001135697.2:c.342T>C	NP_001129169.1:p.Asp114=
NR_135553.1:n.398T>C
XM_011525120.2:c.504T>C	XP_011523422.2:p.Asp168=
XM_011525121.2:c.504T>C	XP_011523423.2:p.Asp168=
XM_011525122.2:c.504T>C	XP_011523424.2:p.Asp168=
XM_011525123.2:c.504T>C	XP_011523425.2:p.Asp168=
XM_011525124.2:c.36T>C	XP_011523426.1:p.Asp12=
XM_024450873.1:c.36T>C	XP_024306641.1:p.Asp12=
XR_002958056.1:n.860T>C
NM_000023.4:c.342T>C MANE Select	NP_000014.1:p.Asp114=
NM_001135697.3:c.342T>C	NP_001129169.1:p.Asp114=
NR_135553.2:n.378T>C