Canonical Allele Identifier: CA104883444

Gene: FAT4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125452811G>T , CM000666.2:g.125452811G>T	GRCh38
NC_000004.11:g.126373966G>T , CM000666.1:g.126373966G>T	GRCh37
NC_000004.10:g.126593416G>T	NCBI36
NG_033865.1:g.141400G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001291303.3:c.11800+1G>T MANE Select	NP_001278232.1:n.11800+1G>T
ENST00000394329.9:c.11800+1G>T MANE Select	ENSP00000377862.4:n.11800+1G>T
NM_001291285.1:c.11800+1G>T	NP_001278214.1:n.11800+1G>T
NM_001291285.2:c.11800+1G>T	NP_001278214.1:n.11800+1G>T
NM_001291285.3:c.11800+1G>T	NP_001278214.1:n.11800+1G>T
NM_001291303.1:c.11800+1G>T	NP_001278232.1:n.11800+1G>T
NM_024582.4:c.11794+1G>T	NP_078858.4:n.11794+1G>T
NM_024582.5:c.11794+1G>T	NP_078858.4:n.11794+1G>T
NM_024582.6:c.11794+1G>T	NP_078858.4:n.11794+1G>T
ENST00000335110.5:c.6688+1G>T	ENSP00000335169.5:n.6688+1G>T
ENST00000394329.7:c.11794+1G>T	ENSP00000377862.3:n.11794+1G>T
ENST00000674496.2:c.6571+1G>T	ENSP00000501473.2:n.6571+1G>T
XM_011532236.1:c.11800+1G>T	XP_011530538.1:n.11800+1G>T
XM_011532236.2:c.11800+1G>T	XP_011530538.1:n.11800+1G>T
XM_011532237.1:c.6571+1G>T	XP_011530539.1:n.6571+1G>T
XM_011532237.2:c.6571+1G>T	XP_011530539.1:n.6571+1G>T