Canonical Allele Identifier: CA291536747
Community Standard Title: NM_000023.4(SGCA):c.643T>C (p.Ser215Pro)
Gene: SGCA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50169150T>C , CM000679.2:g.50169150T>C GRCh38
NC_000017.10:g.48246511T>C , CM000679.1:g.48246511T>C GRCh37
NC_000017.9:g.45601510T>C NCBI36
NG_008889.1:g.8146T>C , LRG_203:g.8146T>C

Transcript Alleles

HGVS Amino-acid Change
NM_000023.4:c.643T>C MANE Select NP_000014.1:p.Ser215Pro
ENST00000262018.8:c.643T>C MANE Select ENSP00000262018.3:p.Ser215Pro
NM_000023.2:c.643T>C , LRG_203t1:c.643T>C NP_000014.1:p.Ser215Pro
NM_000023.3:c.643T>C NP_000014.1:p.Ser215Pro
NM_001135697.1:c.584+578T>C NP_001129169.1:n.584+578T>C
NM_001135697.2:c.584+578T>C NP_001129169.1:n.584+578T>C
NM_001135697.3:c.584+578T>C NP_001129169.1:n.584+578T>C
NR_135553.1:n.699T>C
NR_135553.2:n.679T>C
ENST00000262018.7:c.643T>C ENSP00000262018.3:p.Ser215Pro
ENST00000344627.10:c.584+578T>C ENSP00000345522.6:n.584+578T>C
ENST00000502555.5:c.*302T>C ENSP00000422817.1:n.*302T>C
ENST00000504073.1:c.64+46T>C
ENST00000504073.2:c.597+46T>C ENSP00000422030.2:n.597+46T>C
ENST00000511303.5:c.305+578T>C ENSP00000426104.1:n.305+578T>C
ENST00000511303.6:n.309+578T>C
ENST00000512526.1:c.419+578T>C
ENST00000512526.2:c.575+578T>C ENSP00000426606.2:n.575+578T>C
ENST00000513821.5:c.643T>C ENSP00000426571.1:p.Ser215Pro
ENST00000513942.5:n.375+578T>C
ENST00000682109.1:c.523T>C ENSP00000508041.1:p.Ser175Pro
ENST00000683226.1:n.353T>C
ENST00000683294.1:c.643T>C ENSP00000508134.1:p.Ser215Pro
XM_011525120.1:c.643T>C XP_011523422.1:p.Ser215Pro
XM_011525120.2:c.805T>C XP_011523422.2:p.Ser269Pro
XM_011525121.1:c.597+46T>C XP_011523423.1:n.597+46T>C
XM_011525121.2:c.759+46T>C XP_011523423.2:n.759+46T>C
XM_011525122.1:c.643T>C XP_011523424.1:p.Ser215Pro
XM_011525122.2:c.805T>C XP_011523424.2:p.Ser269Pro
XM_011525123.1:c.584+578T>C XP_011523425.1:n.584+578T>C
XM_011525123.2:c.746+578T>C XP_011523425.2:n.746+578T>C
XM_011525124.1:c.337T>C XP_011523426.1:p.Ser113Pro
XM_011525124.2:c.337T>C XP_011523426.1:p.Ser113Pro
XM_024450873.1:c.337T>C XP_024306641.1:p.Ser113Pro
XR_002958056.1:n.1161T>C
XR_934517.1:n.709T>C