Canonical Allele Identifier: CA2263905275
Gene: SGCA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50167825C= , CM000679.2:g.50167825C= GRCh38
NC_000017.10:g.48245186C= , CM000679.1:g.48245186C= GRCh37
NC_000017.9:g.45600185C= NCBI36
NG_008889.1:g.6821C= , LRG_203:g.6821C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000504073.2:c.312+89C= ENSP00000422030.2:n.312+89C=
ENST00000511303.6:n.38-122C=
ENST00000512526.2:c.303+98C= ENSP00000426606.2:n.303+98C=
ENST00000682109.1:c.192+89C= ENSP00000508041.1:n.192+89C=
ENST00000683226.1:n.22+89C=
ENST00000683294.1:c.312+89C= ENSP00000508134.1:n.312+89C=
ENST00000262018.8:c.312+89C= MANE Select ENSP00000262018.3:n.312+89C=
ENST00000262018.7:c.312+89C= ENSP00000262018.3:n.312+89C=
ENST00000344627.10:c.312+89C= ENSP00000345522.6:n.312+89C=
ENST00000502555.5:c.158-122C= ENSP00000422817.1:n.158-122C=
ENST00000511303.5:c.34-122C= ENSP00000426104.1:n.34-122C=
ENST00000512526.1:c.147+98C=
ENST00000513821.5:c.312+89C= ENSP00000426571.1:n.312+89C=
ENST00000513942.5:n.104-122C=
ENST00000514934.1:c.*19-122C= ENSP00000423168.1:n.*19-122C=
NM_000023.2:c.312+89C= , LRG_203t1:c.312+89C= NP_000014.1:n.312+89C=
NM_001135697.1:c.312+89C= NP_001129169.1:n.312+89C=
XM_011525120.1:c.312+89C= XP_011523422.1:n.312+89C=
XM_011525121.1:c.312+89C= XP_011523423.1:n.312+89C=
XM_011525122.1:c.312+89C= XP_011523424.1:n.312+89C=
XM_011525123.1:c.312+89C= XP_011523425.1:n.312+89C=
XM_011525124.1:c.7-122C= XP_011523426.1:n.7-122C=
XR_934517.1:n.378+89C=
NM_000023.3:c.312+89C= NP_000014.1:n.312+89C=
NM_001135697.2:c.312+89C= NP_001129169.1:n.312+89C=
NR_135553.1:n.368+89C=
XM_011525120.2:c.474+89C= XP_011523422.2:n.474+89C=
XM_011525121.2:c.474+89C= XP_011523423.2:n.474+89C=
XM_011525122.2:c.474+89C= XP_011523424.2:n.474+89C=
XM_011525123.2:c.474+89C= XP_011523425.2:n.474+89C=
XM_011525124.2:c.7-122C= XP_011523426.1:n.7-122C=
XM_024450873.1:c.7-122C= XP_024306641.1:n.7-122C=
XR_002958056.1:n.830+89C=
NM_000023.4:c.312+89C= MANE Select NP_000014.1:n.312+89C=
NM_001135697.3:c.312+89C= NP_001129169.1:n.312+89C=
NR_135553.2:n.348+89C=