Canonical Allele Identifier: CA104862065
Gene: FAT4 HGNC NCBI

Linked Data

dbSNP Id: rs746792200

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.125317655C>T , CM000666.2:g.125317655C>T GRCh38
NC_000004.11:g.126238810C>T , CM000666.1:g.126238810C>T GRCh37
NC_000004.10:g.126458260C>T NCBI36
NG_033865.1:g.6244C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000394329.9:c.1244C>T MANE Select ENSP00000377862.4:p.Pro415Leu
ENST00000674496.2:c.-55+1678C>T ENSP00000501473.2:p.=
ENST00000394329.7:c.1244C>T ENSP00000377862.3:p.Pro415Leu
NM_001291285.1:n.1244C>T NP_001278214.1:p.Pro415Leu
NM_001291303.1:n.1244C>T NP_001278232.1:p.Pro415Leu
NM_024582.4:n.1244C>T NP_078858.4:p.Pro415Leu
XM_011532236.1:c.1244C>T XP_011530538.1:p.Pro415Leu
XM_011532237.1:c.-55+1678C>T XP_011530539.1:p.=
XM_011532236.2:c.1244C>T XP_011530538.1:p.Pro415Leu
XM_011532237.2:c.-55+1678C>T XP_011530539.1:p.=
NM_001291285.2:c.1244C>T NP_001278214.1:p.Pro415Leu
NM_001291303.3:c.1244C>T MANE Select NP_001278232.1:p.Pro415Leu
NM_024582.5:c.1244C>T NP_078858.4:p.Pro415Leu
NM_001291285.3:c.1244C>T NP_001278214.1:p.Pro415Leu
NM_024582.6:c.1244C>T NP_078858.4:p.Pro415Leu