Canonical Allele Identifier: CA358132505

Gene: FAT4

Linked Data

• MyVariant Identifiers: chr4:g.126402727A>C (hg19) ; chr4:g.125481572A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125481572A>C , CM000666.2:g.125481572A>C	GRCh38
NC_000004.11:g.126402727A>C , CM000666.1:g.126402727A>C	GRCh37
NC_000004.10:g.126622177A>C	NCBI36
NG_033865.1:g.170161A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000394329.9:c.12656A>C MANE Select	ENSP00000377862.4:p.Tyr4219Ser
ENST00000674496.2:c.7427A>C	ENSP00000501473.2:p.Tyr2476Ser
ENST00000335110.5:c.7373A>C	ENSP00000335169.5:p.Tyr2458Ser
ENST00000394329.7:c.12650A>C	ENSP00000377862.3:p.Tyr4217Ser
NM_001291285.1:c.12656A>C	NP_001278214.1:p.Tyr4219Ser
NM_001291303.1:c.12656A>C	NP_001278232.1:p.Tyr4219Ser
NM_024582.4:c.12650A>C	NP_078858.4:p.Tyr4217Ser
XM_011532236.1:c.12656A>C	XP_011530538.1:p.Tyr4219Ser
XM_011532237.1:c.7427A>C	XP_011530539.1:p.Tyr2476Ser
XM_011532236.2:c.12656A>C	XP_011530538.1:p.Tyr4219Ser
XM_011532237.2:c.7427A>C	XP_011530539.1:p.Tyr2476Ser
NM_001291285.2:c.12656A>C	NP_001278214.1:p.Tyr4219Ser
NM_001291303.3:c.12656A>C MANE Select	NP_001278232.1:p.Tyr4219Ser
NM_024582.5:c.12650A>C	NP_078858.4:p.Tyr4217Ser
NM_001291285.3:c.12656A>C	NP_001278214.1:p.Tyr4219Ser
NM_024582.6:c.12650A>C	NP_078858.4:p.Tyr4217Ser