Canonical Allele Identifier: CA441367057
Gene: FAT4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.126239756T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.125318601T>C , CM000666.2:g.125318601T>C GRCh38
NC_000004.11:g.126239756T>C , CM000666.1:g.126239756T>C GRCh37
NC_000004.10:g.126459206T>C NCBI36
NG_033865.1:g.7190T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000394329.9:c.2190T>C MANE Select ENSP00000377862.4:p.Ala730=
ENST00000674496.2:c.-55+2624T>C ENSP00000501473.2:n.-55+2624T>C
ENST00000394329.7:c.2190T>C ENSP00000377862.3:p.Ala730=
NM_001291285.1:c.2190T>C NP_001278214.1:p.Ala730=
NM_001291303.1:c.2190T>C NP_001278232.1:p.Ala730=
NM_024582.4:c.2190T>C NP_078858.4:p.Ala730=
XM_011532236.1:c.2190T>C XP_011530538.1:p.Ala730=
XM_011532237.1:c.-55+2624T>C XP_011530539.1:n.-55+2624T>C
XM_011532236.2:c.2190T>C XP_011530538.1:p.Ala730=
XM_011532237.2:c.-55+2624T>C XP_011530539.1:n.-55+2624T>C
NM_001291285.2:c.2190T>C NP_001278214.1:p.Ala730=
NM_001291303.3:c.2190T>C MANE Select NP_001278232.1:p.Ala730=
NM_024582.5:c.2190T>C NP_078858.4:p.Ala730=
NM_001291285.3:c.2190T>C NP_001278214.1:p.Ala730=
NM_024582.6:c.2190T>C NP_078858.4:p.Ala730=