Canonical Allele Identifier: CA358117515
Gene: FAT4 HGNC NCBI

Linked Data

dbSNP Id: rs1730681290

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.125317661T>C , CM000666.2:g.125317661T>C GRCh38
NC_000004.11:g.126238816T>C , CM000666.1:g.126238816T>C GRCh37
NC_000004.10:g.126458266T>C NCBI36
NG_033865.1:g.6250T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000394329.9:c.1250T>C MANE Select ENSP00000377862.4:p.Leu417Pro
ENST00000674496.2:c.-55+1684T>C ENSP00000501473.2:n.-55+1684T>C
ENST00000394329.7:c.1250T>C ENSP00000377862.3:p.Leu417Pro
NM_001291285.1:c.1250T>C NP_001278214.1:p.Leu417Pro
NM_001291303.1:c.1250T>C NP_001278232.1:p.Leu417Pro
NM_024582.4:c.1250T>C NP_078858.4:p.Leu417Pro
XM_011532236.1:c.1250T>C XP_011530538.1:p.Leu417Pro
XM_011532237.1:c.-55+1684T>C XP_011530539.1:n.-55+1684T>C
XM_011532236.2:c.1250T>C XP_011530538.1:p.Leu417Pro
XM_011532237.2:c.-55+1684T>C XP_011530539.1:n.-55+1684T>C
NM_001291285.2:c.1250T>C NP_001278214.1:p.Leu417Pro
NM_001291303.3:c.1250T>C MANE Select NP_001278232.1:p.Leu417Pro
NM_024582.5:c.1250T>C NP_078858.4:p.Leu417Pro
NM_001291285.3:c.1250T>C NP_001278214.1:p.Leu417Pro
NM_024582.6:c.1250T>C NP_078858.4:p.Leu417Pro