Canonical Allele Identifier: CA358976419

Gene: FAT1

Linked Data

• MyVariant Identifiers: chr4:g.187524927G>T (hg19) ; chr4:g.186603773G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186603773G>T , CM000666.2:g.186603773G>T	GRCh38
NC_000004.11:g.187524927G>T , CM000666.1:g.187524927G>T	GRCh37
NC_000004.10:g.187761921G>T	NCBI36
NG_046994.1:g.128143C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000441802.7:c.10753C>A MANE Select	ENSP00000406229.2:p.Gln3585Lys
ENST00000441802.6:c.10753C>A	ENSP00000406229.2:p.Gln3585Lys
ENST00000614102.4:c.10759C>A	ENSP00000479573.1:p.Gln3587Lys
NM_005245.3:c.10753C>A	NP_005236.2:p.Gln3585Lys
XM_005262834.2:c.10753C>A	XP_005262891.1:p.Gln3585Lys
XM_005262835.1:c.10753C>A	XP_005262892.1:p.Gln3585Lys
XM_006714139.2:c.10753C>A	XP_006714202.1:p.Gln3585Lys
XM_005262834.3:c.10753C>A	XP_005262891.1:p.Gln3585Lys
XM_005262835.2:c.10753C>A	XP_005262892.1:p.Gln3585Lys
XM_006714139.3:c.10753C>A	XP_006714202.1:p.Gln3585Lys
NM_005245.4:c.10753C>A MANE Select	NP_005236.2:p.Gln3585Lys