Canonical Allele Identifier: CA104876095

Gene: FAT4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125490371G>A , CM000666.2:g.125490371G>A	GRCh38
NC_000004.11:g.126411526G>A , CM000666.1:g.126411526G>A	GRCh37
NC_000004.10:g.126630976G>A	NCBI36
NG_033865.1:g.178960G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001291303.3:c.13555G>A MANE Select	NP_001278232.1:p.Ala4519Thr
ENST00000394329.9:c.13555G>A MANE Select	ENSP00000377862.4:p.Ala4519Thr
NM_001291285.1:c.13552G>A	NP_001278214.1:p.Ala4518Thr
NM_001291285.2:c.13552G>A	NP_001278214.1:p.Ala4518Thr
NM_001291285.3:c.13552G>A	NP_001278214.1:p.Ala4518Thr
NM_001291303.1:c.13555G>A	NP_001278232.1:p.Ala4519Thr
NM_024582.4:c.13549G>A	NP_078858.4:p.Ala4517Thr
NM_024582.5:c.13549G>A	NP_078858.4:p.Ala4517Thr
NM_024582.6:c.13549G>A	NP_078858.4:p.Ala4517Thr
ENST00000335110.5:c.8272G>A	ENSP00000335169.5:p.Ala2758Thr
ENST00000394329.7:c.13549G>A	ENSP00000377862.3:p.Ala4517Thr
ENST00000674496.2:c.8326G>A	ENSP00000501473.2:p.Ala2776Thr
XM_011532236.1:c.13555G>A	XP_011530538.1:p.Ala4519Thr
XM_011532236.2:c.13555G>A	XP_011530538.1:p.Ala4519Thr
XM_011532237.1:c.8326G>A	XP_011530539.1:p.Ala2776Thr
XM_011532237.2:c.8326G>A	XP_011530539.1:p.Ala2776Thr