Canonical Allele Identifier: CA447414385

Gene: FAT2 SLC36A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151507548C>T , CM000667.2:g.151507548C>T	GRCh38
NC_000005.9:g.150887109C>T , CM000667.1:g.150887109C>T	GRCh37
NC_000005.8:g.150867302C>T	NCBI36
NG_046979.1:g.149593G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261800.6:c.12123G>A (FAT2) MANE Select	ENSP00000261800.5:p.Arg4041=
ENST00000261800.5:c.12123G>A (FAT2)	ENSP00000261800.5:p.Arg4041=
ENST00000520200.5:c.2440G>A (FAT2)
NM_001447.2:c.12123G>A (FAT2)	NP_001438.1:p.Arg4041=
XM_006714761.2:c.12123G>A (FAT2)	XP_006714824.1:p.Arg4041=
XM_011537595.1:c.1252+28059C>T (SLC36A1)	XP_011535897.1:n.1252+28059C>T
XM_011537598.1:c.12123G>A (FAT2)	XP_011535900.1:p.Arg4041=
XM_011537599.1:c.12123G>A (FAT2)	XP_011535901.1:p.Arg4041=
XM_011537600.1:c.12123G>A (FAT2)	XP_011535902.1:p.Arg4041=
XM_011537601.1:c.12123G>A (FAT2)	XP_011535903.1:p.Arg4041=
XM_011537602.1:c.12123G>A (FAT2)	XP_011535904.1:p.Arg4041=
XM_011537603.1:c.12123G>A (FAT2)	XP_011535905.1:p.Arg4041=
XM_011537604.1:c.*20G>A (FAT2)	XP_011535906.1:n.*20G>A
XR_944309.1:n.1551+28059C>T (SLC36A1)
XM_006714761.3:c.12123G>A (FAT2)	XP_006714824.1:p.Arg4041=
XM_011537595.2:c.1177+28059C>T (SLC36A1)	XP_011535897.2:n.1177+28059C>T
XM_011537600.2:c.12123G>A (FAT2)	XP_011535902.1:p.Arg4041=
XM_011537603.2:c.12123G>A (FAT2)	XP_011535905.1:p.Arg4041=
XM_017009217.1:c.1159+28059C>T (SLC36A1)	XP_016864706.1:n.1159+28059C>T
XM_017009219.2:c.925+28059C>T (SLC36A1)	XP_016864708.1:n.925+28059C>T
XM_017009224.1:c.12123G>A (FAT2)	XP_016864713.1:p.Arg4041=
XM_017009225.1:c.12123G>A (FAT2)	XP_016864714.1:p.Arg4041=
XM_024446001.1:c.1159+28059C>T (SLC36A1)	XP_024301769.1:n.1159+28059C>T
XR_001742039.1:n.12269G>A (FAT2)
NM_001447.3:c.12123G>A (FAT2) MANE Select	NP_001438.1:p.Arg4041=