Canonical Allele Identifier: CA129940785

Gene: FAT2 SLC36A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151531381T>C , CM000667.2:g.151531381T>C	GRCh38
NC_000005.9:g.150910942T>C , CM000667.1:g.150910942T>C	GRCh37
NC_000005.8:g.150891135T>C	NCBI36
NG_046979.1:g.125760A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261800.6:c.9811+206A>G (FAT2) MANE Select	ENSP00000261800.5:n.9811+206A>G
ENST00000261800.5:c.9811+206A>G (FAT2)	ENSP00000261800.5:n.9811+206A>G
ENST00000520200.5:c.386+206A>G (FAT2)
NM_001447.2:c.9811+206A>G (FAT2)	NP_001438.1:n.9811+206A>G
XM_006714761.2:c.9811+206A>G (FAT2)	XP_006714824.1:n.9811+206A>G
XM_011537595.1:c.1253-7872T>C (SLC36A1)	XP_011535897.1:n.1253-7872T>C
XM_011537598.1:c.9811+206A>G (FAT2)	XP_011535900.1:n.9811+206A>G
XM_011537599.1:c.9811+206A>G (FAT2)	XP_011535901.1:n.9811+206A>G
XM_011537600.1:c.9811+206A>G (FAT2)	XP_011535902.1:n.9811+206A>G
XM_011537601.1:c.9811+206A>G (FAT2)	XP_011535903.1:n.9811+206A>G
XM_011537602.1:c.9811+206A>G (FAT2)	XP_011535904.1:n.9811+206A>G
XM_011537603.1:c.9811+206A>G (FAT2)	XP_011535905.1:n.9811+206A>G
XM_011537604.1:c.9811+206A>G (FAT2)	XP_011535906.1:n.9811+206A>G
XM_011537605.1:c.9811+206A>G (FAT2)	XP_011535907.1:n.9811+206A>G
XR_944309.1:n.1552-7872T>C (SLC36A1)
XM_006714761.3:c.9811+206A>G (FAT2)	XP_006714824.1:n.9811+206A>G
XM_011537595.2:c.1178-7872T>C (SLC36A1)	XP_011535897.2:n.1178-7872T>C
XM_011537600.2:c.9811+206A>G (FAT2)	XP_011535902.1:n.9811+206A>G
XM_011537603.2:c.9811+206A>G (FAT2)	XP_011535905.1:n.9811+206A>G
XM_017009217.1:c.1160-7872T>C (SLC36A1)	XP_016864706.1:n.1160-7872T>C
XM_017009219.2:c.926-7872T>C (SLC36A1)	XP_016864708.1:n.926-7872T>C
XM_017009224.1:c.9811+206A>G (FAT2)	XP_016864713.1:n.9811+206A>G
XM_017009225.1:c.9811+206A>G (FAT2)	XP_016864714.1:n.9811+206A>G
XM_024446001.1:c.1160-7872T>C (SLC36A1)	XP_024301769.1:n.1160-7872T>C
XR_001742039.1:n.10399+206A>G (FAT2)
NM_001447.3:c.9811+206A>G (FAT2) MANE Select	NP_001438.1:n.9811+206A>G