Canonical Allele Identifier: CA2263906510
Gene: SGCA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50170182A= , CM000679.2:g.50170182A= GRCh38
NC_000017.10:g.48247543A= , CM000679.1:g.48247543A= GRCh37
NC_000017.9:g.45602542A= NCBI36
NG_008889.1:g.9178A= , LRG_203:g.9178A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000504073.2:c.637A= ENSP00000422030.2:p.Thr213=
ENST00000511303.6:n.310-458A=
ENST00000512526.2:c.576-458A= ENSP00000426606.2:n.576-458A=
ENST00000682109.1:c.667A= ENSP00000508041.1:p.Thr223=
ENST00000683226.1:n.1385A=
ENST00000683294.1:c.*53A= ENSP00000508134.1:n.*53A=
ENST00000683544.1:n.153A=
ENST00000262018.8:c.787A= MANE Select ENSP00000262018.3:p.Thr263=
ENST00000262018.7:c.787A= ENSP00000262018.3:p.Thr263=
ENST00000344627.10:c.585-458A= ENSP00000345522.6:n.585-458A=
ENST00000504073.1:c.104A=
ENST00000511303.5:c.306-458A= ENSP00000426104.1:n.306-458A=
ENST00000512526.1:c.420-458A=
ENST00000513821.5:c.748-458A= ENSP00000426571.1:n.748-458A=
ENST00000513942.5:n.376-458A=
NM_000023.2:c.787A= , LRG_203t1:c.787A= NP_000014.1:p.Thr263=
NM_001135697.1:c.585-458A= NP_001129169.1:n.585-458A=
XM_011525120.1:c.787A= XP_011523422.1:p.Thr263=
XM_011525121.1:c.637A= XP_011523423.1:p.Thr213=
XM_011525122.1:c.748-458A= XP_011523424.1:n.748-458A=
XM_011525123.1:c.585-458A= XP_011523425.1:n.585-458A=
XM_011525124.1:c.481A= XP_011523426.1:p.Thr161=
XR_934517.1:n.814-458A=
NM_000023.3:c.787A= NP_000014.1:p.Thr263=
NM_001135697.2:c.585-458A= NP_001129169.1:n.585-458A=
NR_135553.1:n.804-458A=
XM_011525120.2:c.949A= XP_011523422.2:p.Thr317=
XM_011525121.2:c.799A= XP_011523423.2:p.Thr267=
XM_011525122.2:c.910-458A= XP_011523424.2:n.910-458A=
XM_011525123.2:c.747-458A= XP_011523425.2:n.747-458A=
XM_011525124.2:c.481A= XP_011523426.1:p.Thr161=
XM_024450873.1:c.481A= XP_024306641.1:p.Thr161=
XR_002958056.1:n.1384A=
NM_000023.4:c.787A= MANE Select NP_000014.1:p.Thr263=
NM_001135697.3:c.585-458A= NP_001129169.1:n.585-458A=
NR_135553.2:n.784-458A=