Canonical Allele Identifier: CA2672011574

Gene: FAT4

Linked Data

• gnomAD v4: 4-125468881-TGGGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125468882_125468885del , CM000666.2:g.125468882_125468885del	GRCh38
NC_000004.11:g.126390037_126390040del , CM000666.1:g.126390037_126390040del	GRCh37
NC_000004.10:g.126609487_126609490del	NCBI36
NG_033865.1:g.157471_157474del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394329.9:c.12213+63_12213+66del MANE Select	ENSP00000377862.4:n.12213+63_12213+66del
ENST00000674496.2:c.6984+63_6984+66del	ENSP00000501473.2:n.6984+63_6984+66del
ENST00000335110.5:c.6996+63_6996+66del	ENSP00000335169.5:n.6996+63_6996+66del
ENST00000394329.7:c.12207+63_12207+66del	ENSP00000377862.3:n.12207+63_12207+66del
NM_001291285.1:c.12213+63_12213+66del	NP_001278214.1:n.12213+63_12213+66del
NM_001291303.1:c.12213+63_12213+66del	NP_001278232.1:n.12213+63_12213+66del
NM_024582.4:c.12207+63_12207+66del	NP_078858.4:n.12207+63_12207+66del
XM_011532236.1:c.12213+63_12213+66del	XP_011530538.1:n.12213+63_12213+66del
XM_011532237.1:c.6984+63_6984+66del	XP_011530539.1:n.6984+63_6984+66del
XM_011532236.2:c.12213+63_12213+66del	XP_011530538.1:n.12213+63_12213+66del
XM_011532237.2:c.6984+63_6984+66del	XP_011530539.1:n.6984+63_6984+66del
NM_001291285.2:c.12213+63_12213+66del	NP_001278214.1:n.12213+63_12213+66del
NM_001291303.3:c.12213+63_12213+66del MANE Select	NP_001278232.1:n.12213+63_12213+66del
NM_024582.5:c.12207+63_12207+66del	NP_078858.4:n.12207+63_12207+66del
NM_001291285.3:c.12213+63_12213+66del	NP_001278214.1:n.12213+63_12213+66del
NM_024582.6:c.12207+63_12207+66del	NP_078858.4:n.12207+63_12207+66del