Canonical Allele Identifier: CA358132509

Gene: FAT4

Linked Data

• MyVariant Identifiers: chr4:g.126402728C>G (hg19) ; chr4:g.125481573C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125481573C>G , CM000666.2:g.125481573C>G	GRCh38
NC_000004.11:g.126402728C>G , CM000666.1:g.126402728C>G	GRCh37
NC_000004.10:g.126622178C>G	NCBI36
NG_033865.1:g.170162C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000394329.9:c.12657C>G MANE Select	ENSP00000377862.4:p.Tyr4219Ter
ENST00000674496.2:c.7428C>G	ENSP00000501473.2:p.Tyr2476Ter
ENST00000335110.5:c.7374C>G	ENSP00000335169.5:p.Tyr2458Ter
ENST00000394329.7:c.12651C>G	ENSP00000377862.3:p.Tyr4217Ter
NM_001291285.1:c.12657C>G	NP_001278214.1:p.Tyr4219Ter
NM_001291303.1:c.12657C>G	NP_001278232.1:p.Tyr4219Ter
NM_024582.4:c.12651C>G	NP_078858.4:p.Tyr4217Ter
XM_011532236.1:c.12657C>G	XP_011530538.1:p.Tyr4219Ter
XM_011532237.1:c.7428C>G	XP_011530539.1:p.Tyr2476Ter
XM_011532236.2:c.12657C>G	XP_011530538.1:p.Tyr4219Ter
XM_011532237.2:c.7428C>G	XP_011530539.1:p.Tyr2476Ter
NM_001291285.2:c.12657C>G	NP_001278214.1:p.Tyr4219Ter
NM_001291303.3:c.12657C>G MANE Select	NP_001278232.1:p.Tyr4219Ter
NM_024582.5:c.12651C>G	NP_078858.4:p.Tyr4217Ter
NM_001291285.3:c.12657C>G	NP_001278214.1:p.Tyr4219Ter
NM_024582.6:c.12651C>G	NP_078858.4:p.Tyr4217Ter