Canonical Allele Identifier: CA441366625
Gene: FAT4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.126238715G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.125317560G>C , CM000666.2:g.125317560G>C GRCh38
NC_000004.11:g.126238715G>C , CM000666.1:g.126238715G>C GRCh37
NC_000004.10:g.126458165G>C NCBI36
NG_033865.1:g.6149G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000394329.9:c.1149G>C MANE Select ENSP00000377862.4:p.Thr383=
ENST00000674496.2:c.-55+1583G>C ENSP00000501473.2:n.-55+1583G>C
ENST00000394329.7:c.1149G>C ENSP00000377862.3:p.Thr383=
NM_001291285.1:c.1149G>C NP_001278214.1:p.Thr383=
NM_001291303.1:c.1149G>C NP_001278232.1:p.Thr383=
NM_024582.4:c.1149G>C NP_078858.4:p.Thr383=
XM_011532236.1:c.1149G>C XP_011530538.1:p.Thr383=
XM_011532237.1:c.-55+1583G>C XP_011530539.1:n.-55+1583G>C
XM_011532236.2:c.1149G>C XP_011530538.1:p.Thr383=
XM_011532237.2:c.-55+1583G>C XP_011530539.1:n.-55+1583G>C
NM_001291285.2:c.1149G>C NP_001278214.1:p.Thr383=
NM_001291303.3:c.1149G>C MANE Select NP_001278232.1:p.Thr383=
NM_024582.5:c.1149G>C NP_078858.4:p.Thr383=
NM_001291285.3:c.1149G>C NP_001278214.1:p.Thr383=
NM_024582.6:c.1149G>C NP_078858.4:p.Thr383=