Canonical Allele Identifier: CA3519801

Gene: FAT2 SLC36A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151507337T>C , CM000667.2:g.151507337T>C	GRCh38
NC_000005.9:g.150886898T>C , CM000667.1:g.150886898T>C	GRCh37
NC_000005.8:g.150867091T>C	NCBI36
NG_046979.1:g.149804A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001447.3:c.12334A>G (FAT2) MANE Select	NP_001438.1:p.Asn4112Asp
ENST00000261800.6:c.12334A>G (FAT2) MANE Select	ENSP00000261800.5:p.Asn4112Asp
NM_001447.2:c.12334A>G (FAT2)	NP_001438.1:p.Asn4112Asp
ENST00000261800.5:c.12334A>G (FAT2)	ENSP00000261800.5:p.Asn4112Asp
ENST00000520200.5:c.2651A>G (FAT2)
XM_006714761.2:c.12334A>G (FAT2)	XP_006714824.1:p.Asn4112Asp
XM_006714761.3:c.12334A>G (FAT2)	XP_006714824.1:p.Asn4112Asp
XM_011537595.1:c.1252+27848T>C (SLC36A1)	XP_011535897.1:n.1252+27848T>C
XM_011537595.2:c.1177+27848T>C (SLC36A1)	XP_011535897.2:n.1177+27848T>C
XM_011537598.1:c.12334A>G (FAT2)	XP_011535900.1:p.Asn4112Asp
XM_011537599.1:c.12334A>G (FAT2)	XP_011535901.1:p.Asn4112Asp
XM_011537600.1:c.12334A>G (FAT2)	XP_011535902.1:p.Asn4112Asp
XM_011537600.2:c.12334A>G (FAT2)	XP_011535902.1:p.Asn4112Asp
XM_011537601.1:c.12334A>G (FAT2)	XP_011535903.1:p.Asn4112Asp
XM_011537602.1:c.12334A>G (FAT2)	XP_011535904.1:p.Asn4112Asp
XM_011537603.1:c.12334A>G (FAT2)	XP_011535905.1:p.Asn4112Asp
XM_011537603.2:c.12334A>G (FAT2)	XP_011535905.1:p.Asn4112Asp
XM_017009217.1:c.1159+27848T>C (SLC36A1)	XP_016864706.1:n.1159+27848T>C
XM_017009219.2:c.925+27848T>C (SLC36A1)	XP_016864708.1:n.925+27848T>C
XM_017009224.1:c.12334A>G (FAT2)	XP_016864713.1:p.Asn4112Asp
XM_017009225.1:c.12334A>G (FAT2)	XP_016864714.1:p.Asn4112Asp
XM_024446001.1:c.1159+27848T>C (SLC36A1)	XP_024301769.1:n.1159+27848T>C
XR_001742039.1:n.12480A>G (FAT2)
XR_944309.1:n.1551+27848T>C (SLC36A1)