Canonical Allele Identifier: CA2263905438
Gene: SGCA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50168034G= , CM000679.2:g.50168034G= GRCh38
NC_000017.10:g.48245395G= , CM000679.1:g.48245395G= GRCh37
NC_000017.9:g.45600394G= NCBI36
NG_008889.1:g.7030G= , LRG_203:g.7030G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000504073.2:c.385+15G= ENSP00000422030.2:n.385+15G=
ENST00000511303.6:n.110+15G=
ENST00000512526.2:c.376+15G= ENSP00000426606.2:n.376+15G=
ENST00000682109.1:c.265+15G= ENSP00000508041.1:n.265+15G=
ENST00000683226.1:n.95+15G=
ENST00000683294.1:c.385+15G= ENSP00000508134.1:n.385+15G=
ENST00000262018.8:c.385+15G= MANE Select ENSP00000262018.3:n.385+15G=
ENST00000262018.7:c.385+15G= ENSP00000262018.3:n.385+15G=
ENST00000344627.10:c.385+15G= ENSP00000345522.6:n.385+15G=
ENST00000502555.5:c.*44+15G= ENSP00000422817.1:n.*44+15G=
ENST00000511303.5:c.106+15G= ENSP00000426104.1:n.106+15G=
ENST00000512526.1:c.220+15G=
ENST00000513821.5:c.385+15G= ENSP00000426571.1:n.385+15G=
ENST00000513942.5:n.176+15G=
ENST00000514934.1:c.*91+15G= ENSP00000423168.1:n.*91+15G=
NM_000023.2:c.385+15G= , LRG_203t1:c.385+15G= NP_000014.1:n.385+15G=
NM_001135697.1:c.385+15G= NP_001129169.1:n.385+15G=
XM_011525120.1:c.385+15G= XP_011523422.1:n.385+15G=
XM_011525121.1:c.385+15G= XP_011523423.1:n.385+15G=
XM_011525122.1:c.385+15G= XP_011523424.1:n.385+15G=
XM_011525123.1:c.385+15G= XP_011523425.1:n.385+15G=
XM_011525124.1:c.79+15G= XP_011523426.1:n.79+15G=
XR_934517.1:n.451+15G=
NM_000023.3:c.385+15G= NP_000014.1:n.385+15G=
NM_001135697.2:c.385+15G= NP_001129169.1:n.385+15G=
NR_135553.1:n.441+15G=
XM_011525120.2:c.547+15G= XP_011523422.2:n.547+15G=
XM_011525121.2:c.547+15G= XP_011523423.2:n.547+15G=
XM_011525122.2:c.547+15G= XP_011523424.2:n.547+15G=
XM_011525123.2:c.547+15G= XP_011523425.2:n.547+15G=
XM_011525124.2:c.79+15G= XP_011523426.1:n.79+15G=
XM_024450873.1:c.79+15G= XP_024306641.1:n.79+15G=
XR_002958056.1:n.903+15G=
NM_000023.4:c.385+15G= MANE Select NP_000014.1:n.385+15G=
NM_001135697.3:c.385+15G= NP_001129169.1:n.385+15G=
NR_135553.2:n.421+15G=