Canonical Allele Identifier: CA358135542

Gene: FAT4

Linked Data

• MyVariant Identifiers: chr4:g.126355581G>C (hg19) ; chr4:g.125434426G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125434426G>C , CM000666.2:g.125434426G>C	GRCh38
NC_000004.11:g.126355581G>C , CM000666.1:g.126355581G>C	GRCh37
NC_000004.10:g.126575031G>C	NCBI36
NG_033865.1:g.123015G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394329.9:c.7199+1G>C MANE Select	ENSP00000377862.4:n.7199+1G>C
ENST00000674496.2:c.1970+1G>C	ENSP00000501473.2:n.1970+1G>C
ENST00000335110.5:c.2093+1G>C	ENSP00000335169.5:n.2093+1G>C
ENST00000394329.7:c.7199+1G>C	ENSP00000377862.3:n.7199+1G>C
NM_001291285.1:c.7199+1G>C	NP_001278214.1:n.7199+1G>C
NM_001291303.1:c.7199+1G>C	NP_001278232.1:n.7199+1G>C
NM_024582.4:c.7199+1G>C	NP_078858.4:n.7199+1G>C
XM_011532236.1:c.7199+1G>C	XP_011530538.1:n.7199+1G>C
XM_011532237.1:c.1970+1G>C	XP_011530539.1:n.1970+1G>C
XM_011532236.2:c.7199+1G>C	XP_011530538.1:n.7199+1G>C
XM_011532237.2:c.1970+1G>C	XP_011530539.1:n.1970+1G>C
NM_001291285.2:c.7199+1G>C	NP_001278214.1:n.7199+1G>C
NM_001291303.3:c.7199+1G>C MANE Select	NP_001278232.1:n.7199+1G>C
NM_024582.5:c.7199+1G>C	NP_078858.4:n.7199+1G>C
NM_001291285.3:c.7199+1G>C	NP_001278214.1:n.7199+1G>C
NM_024582.6:c.7199+1G>C	NP_078858.4:n.7199+1G>C