Canonical Allele Identifier: CA358132524

Gene: FAT4

Linked Data

• dbSNP Id: rs762857799
• MyVariant Identifiers: chr4:g.126402734G>C (hg19) ; chr4:g.125481579G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125481579G>C , CM000666.2:g.125481579G>C	GRCh38
NC_000004.11:g.126402734G>C , CM000666.1:g.126402734G>C	GRCh37
NC_000004.10:g.126622184G>C	NCBI36
NG_033865.1:g.170168G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394329.9:c.12663G>C MANE Select	ENSP00000377862.4:p.Met4221Ile
ENST00000674496.2:c.7434G>C	ENSP00000501473.2:p.Met2478Ile
ENST00000335110.5:c.7380G>C	ENSP00000335169.5:p.Met2460Ile
ENST00000394329.7:c.12657G>C	ENSP00000377862.3:p.Met4219Ile
NM_001291285.1:c.12663G>C	NP_001278214.1:p.Met4221Ile
NM_001291303.1:c.12663G>C	NP_001278232.1:p.Met4221Ile
NM_024582.4:c.12657G>C	NP_078858.4:p.Met4219Ile
XM_011532236.1:c.12663G>C	XP_011530538.1:p.Met4221Ile
XM_011532237.1:c.7434G>C	XP_011530539.1:p.Met2478Ile
XM_011532236.2:c.12663G>C	XP_011530538.1:p.Met4221Ile
XM_011532237.2:c.7434G>C	XP_011530539.1:p.Met2478Ile
NM_001291285.2:c.12663G>C	NP_001278214.1:p.Met4221Ile
NM_001291303.3:c.12663G>C MANE Select	NP_001278232.1:p.Met4221Ile
NM_024582.5:c.12657G>C	NP_078858.4:p.Met4219Ile
NM_001291285.3:c.12663G>C	NP_001278214.1:p.Met4221Ile
NM_024582.6:c.12657G>C	NP_078858.4:p.Met4219Ile