Canonical Allele Identifier: CA3521208

Gene: FAT2 SLC36A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151545208G>A , CM000667.2:g.151545208G>A	GRCh38
NC_000005.9:g.150924769G>A , CM000667.1:g.150924769G>A	GRCh37
NC_000005.8:g.150904962G>A	NCBI36
NG_046979.1:g.111933C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001447.3:c.5919C>T (FAT2) MANE Select	NP_001438.1:p.Tyr1973=
ENST00000261800.6:c.5919C>T (FAT2) MANE Select	ENSP00000261800.5:p.Tyr1973=
NM_001447.2:c.5919C>T (FAT2)	NP_001438.1:p.Tyr1973=
ENST00000261800.5:c.5919C>T (FAT2)	ENSP00000261800.5:p.Tyr1973=
XM_006714761.2:c.5919C>T (FAT2)	XP_006714824.1:p.Tyr1973=
XM_006714761.3:c.5919C>T (FAT2)	XP_006714824.1:p.Tyr1973=
XM_011537595.2:c.1220+5913G>A (SLC36A1)	XP_011535897.2:n.1220+5913G>A
XM_011537598.1:c.5919C>T (FAT2)	XP_011535900.1:p.Tyr1973=
XM_011537599.1:c.5919C>T (FAT2)	XP_011535901.1:p.Tyr1973=
XM_011537600.1:c.5919C>T (FAT2)	XP_011535902.1:p.Tyr1973=
XM_011537600.2:c.5919C>T (FAT2)	XP_011535902.1:p.Tyr1973=
XM_011537601.1:c.5919C>T (FAT2)	XP_011535903.1:p.Tyr1973=
XM_011537602.1:c.5919C>T (FAT2)	XP_011535904.1:p.Tyr1973=
XM_011537603.1:c.5919C>T (FAT2)	XP_011535905.1:p.Tyr1973=
XM_011537603.2:c.5919C>T (FAT2)	XP_011535905.1:p.Tyr1973=
XM_011537604.1:c.5919C>T (FAT2)	XP_011535906.1:p.Tyr1973=
XM_011537605.1:c.5919C>T (FAT2)	XP_011535907.1:p.Tyr1973=
XM_011537606.1:c.5919C>T (FAT2)	XP_011535908.1:p.Tyr1973=
XM_017009217.1:c.1202+5913G>A (SLC36A1)	XP_016864706.1:n.1202+5913G>A
XM_017009224.1:c.5919C>T (FAT2)	XP_016864713.1:p.Tyr1973=
XM_017009225.1:c.5919C>T (FAT2)	XP_016864714.1:p.Tyr1973=
XM_017009227.1:c.5919C>T (FAT2)	XP_016864716.1:p.Tyr1973=
XM_024446001.1:c.1202+5913G>A (SLC36A1)	XP_024301769.1:n.1202+5913G>A
XR_001742039.1:n.6507C>T (FAT2)
XR_002956152.1:n.6507C>T (FAT2)
XR_944309.1:n.1594+5913G>A (SLC36A1)
XR_944310.1:n.6482C>T (FAT2)