Canonical Allele Identifier: CA358128171

Gene: FAT4

Linked Data

• dbSNP Id: rs1213045395
• gnomAD v2: 4-126389811-A-G
• gnomAD v3: 4-125468656-A-G
• gnomAD v4: 4-125468656-A-G
• MyVariant Identifiers: chr4:g.126389811A>G (hg19) ; chr4:g.125468656A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125468656A>G , CM000666.2:g.125468656A>G	GRCh38
NC_000004.11:g.126389811A>G , CM000666.1:g.126389811A>G	GRCh37
NC_000004.10:g.126609261A>G	NCBI36
NG_033865.1:g.157245A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394329.9:c.12050A>G MANE Select	ENSP00000377862.4:p.Tyr4017Cys
ENST00000674496.2:c.6821A>G	ENSP00000501473.2:p.Tyr2274Cys
ENST00000335110.5:c.6833A>G	ENSP00000335169.5:p.Tyr2278Cys
ENST00000394329.7:c.12044A>G	ENSP00000377862.3:p.Tyr4015Cys
NM_001291285.1:c.12050A>G	NP_001278214.1:p.Tyr4017Cys
NM_001291303.1:c.12050A>G	NP_001278232.1:p.Tyr4017Cys
NM_024582.4:c.12044A>G	NP_078858.4:p.Tyr4015Cys
XM_011532236.1:c.12050A>G	XP_011530538.1:p.Tyr4017Cys
XM_011532237.1:c.6821A>G	XP_011530539.1:p.Tyr2274Cys
XM_011532236.2:c.12050A>G	XP_011530538.1:p.Tyr4017Cys
XM_011532237.2:c.6821A>G	XP_011530539.1:p.Tyr2274Cys
NM_001291285.2:c.12050A>G	NP_001278214.1:p.Tyr4017Cys
NM_001291303.3:c.12050A>G MANE Select	NP_001278232.1:p.Tyr4017Cys
NM_024582.5:c.12044A>G	NP_078858.4:p.Tyr4015Cys
NM_001291285.3:c.12050A>G	NP_001278214.1:p.Tyr4017Cys
NM_024582.6:c.12044A>G	NP_078858.4:p.Tyr4015Cys