Canonical Allele Identifier: CA400181279

Gene: SGCA

Linked Data

• MyVariant Identifiers: chr17:g.48247512G>C (hg19) ; chr17:g.50170151G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50170151G>C , CM000679.2:g.50170151G>C	GRCh38
NC_000017.10:g.48247512G>C , CM000679.1:g.48247512G>C	GRCh37
NC_000017.9:g.45602511G>C	NCBI36
NG_008889.1:g.9147G>C , LRG_203:g.9147G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504073.2:c.606G>C	ENSP00000422030.2:p.Lys202Asn
ENST00000511303.6:n.310-489G>C
ENST00000512526.2:c.576-489G>C	ENSP00000426606.2:n.576-489G>C
ENST00000682109.1:c.636G>C	ENSP00000508041.1:p.Lys212Asn
ENST00000683226.1:n.1354G>C
ENST00000683294.1:c.*22G>C	ENSP00000508134.1:n.*22G>C
ENST00000683544.1:n.122G>C
ENST00000262018.8:c.756G>C MANE Select	ENSP00000262018.3:p.Lys252Asn
ENST00000262018.7:c.756G>C	ENSP00000262018.3:p.Lys252Asn
ENST00000344627.10:c.585-489G>C	ENSP00000345522.6:n.585-489G>C
ENST00000504073.1:c.73G>C
ENST00000511303.5:c.306-489G>C	ENSP00000426104.1:n.306-489G>C
ENST00000512526.1:c.420-489G>C
ENST00000513821.5:c.748-489G>C	ENSP00000426571.1:n.748-489G>C
ENST00000513942.5:n.376-489G>C
NM_000023.2:c.756G>C , LRG_203t1:c.756G>C	NP_000014.1:p.Lys252Asn
NM_001135697.1:c.585-489G>C	NP_001129169.1:n.585-489G>C
XM_011525120.1:c.756G>C	XP_011523422.1:p.Lys252Asn
XM_011525121.1:c.606G>C	XP_011523423.1:p.Lys202Asn
XM_011525122.1:c.748-489G>C	XP_011523424.1:n.748-489G>C
XM_011525123.1:c.585-489G>C	XP_011523425.1:n.585-489G>C
XM_011525124.1:c.450G>C	XP_011523426.1:p.Lys150Asn
XR_934517.1:n.814-489G>C
NM_000023.3:c.756G>C	NP_000014.1:p.Lys252Asn
NM_001135697.2:c.585-489G>C	NP_001129169.1:n.585-489G>C
NR_135553.1:n.804-489G>C
XM_011525120.2:c.918G>C	XP_011523422.2:p.Lys306Asn
XM_011525121.2:c.768G>C	XP_011523423.2:p.Lys256Asn
XM_011525122.2:c.910-489G>C	XP_011523424.2:n.910-489G>C
XM_011525123.2:c.747-489G>C	XP_011523425.2:n.747-489G>C
XM_011525124.2:c.450G>C	XP_011523426.1:p.Lys150Asn
XM_024450873.1:c.450G>C	XP_024306641.1:p.Lys150Asn
XR_002958056.1:n.1353G>C
NM_000023.4:c.756G>C MANE Select	NP_000014.1:p.Lys252Asn
NM_001135697.3:c.585-489G>C	NP_001129169.1:n.585-489G>C
NR_135553.2:n.784-489G>C