Canonical Allele Identifier: CA2263906460
Gene: SGCA HGNC NCBI

Linked Data

dbSNP Id: rs1598270136

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50170090A>C , CM000679.2:g.50170090A>C GRCh38
NC_000017.10:g.48247451A>C , CM000679.1:g.48247451A>C GRCh37
NC_000017.9:g.45602450A>C NCBI36
NG_008889.1:g.9086A>C , LRG_203:g.9086A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000504073.2:c.598-53A>C ENSP00000422030.2:n.598-53A>C
ENST00000511303.6:n.310-550A>C
ENST00000512526.2:c.576-550A>C ENSP00000426606.2:n.576-550A>C
ENST00000682109.1:c.628-53A>C ENSP00000508041.1:n.628-53A>C
ENST00000683226.1:n.1293A>C
ENST00000683294.1:c.774A>C ENSP00000508134.1:p.Gly258=
ENST00000683544.1:n.61A>C
ENST00000262018.8:c.748-53A>C MANE Select ENSP00000262018.3:n.748-53A>C
ENST00000262018.7:c.748-53A>C ENSP00000262018.3:n.748-53A>C
ENST00000344627.10:c.585-550A>C ENSP00000345522.6:n.585-550A>C
ENST00000504073.1:c.65-53A>C
ENST00000511303.5:c.306-550A>C ENSP00000426104.1:n.306-550A>C
ENST00000512526.1:c.420-550A>C
ENST00000513821.5:c.748-550A>C ENSP00000426571.1:n.748-550A>C
ENST00000513942.5:n.376-550A>C
NM_000023.2:c.748-53A>C , LRG_203t1:c.748-53A>C NP_000014.1:n.748-53A>C
NM_001135697.1:c.585-550A>C NP_001129169.1:n.585-550A>C
XM_011525120.1:c.748-53A>C XP_011523422.1:n.748-53A>C
XM_011525121.1:c.598-53A>C XP_011523423.1:n.598-53A>C
XM_011525122.1:c.748-550A>C XP_011523424.1:n.748-550A>C
XM_011525123.1:c.585-550A>C XP_011523425.1:n.585-550A>C
XM_011525124.1:c.442-53A>C XP_011523426.1:n.442-53A>C
XR_934517.1:n.814-550A>C
NM_000023.3:c.748-53A>C NP_000014.1:n.748-53A>C
NM_001135697.2:c.585-550A>C NP_001129169.1:n.585-550A>C
NR_135553.1:n.804-550A>C
XM_011525120.2:c.910-53A>C XP_011523422.2:n.910-53A>C
XM_011525121.2:c.760-53A>C XP_011523423.2:n.760-53A>C
XM_011525122.2:c.910-550A>C XP_011523424.2:n.910-550A>C
XM_011525123.2:c.747-550A>C XP_011523425.2:n.747-550A>C
XM_011525124.2:c.442-53A>C XP_011523426.1:n.442-53A>C
XM_024450873.1:c.442-53A>C XP_024306641.1:n.442-53A>C
XR_002958056.1:n.1292A>C
NM_000023.4:c.748-53A>C MANE Select NP_000014.1:n.748-53A>C
NM_001135697.3:c.585-550A>C NP_001129169.1:n.585-550A>C
NR_135553.2:n.784-550A>C