Canonical Allele Identifier: CA1660115286

Gene: FABP7

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.122780399C= , CM000668.2:g.122780399C=	GRCh38
NC_000006.11:g.123101544C= , CM000668.1:g.123101544C=	GRCh37
NC_000006.10:g.123143243C=	NCBI36
NG_050619.1:g.36199C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000368444.8:c.182C= MANE Select	ENSP00000357429.3:p.Thr61=
ENST00000356535.4:c.182C=	ENSP00000348931.4:p.Thr61=
ENST00000368444.7:c.182C=	ENSP00000357429.3:p.Thr61=
NM_001446.3:c.182C=	NP_001437.1:p.Thr61=
XM_005266858.2:c.182C=	XP_005266915.1:p.Thr61=
NM_001319039.1:c.182C=	NP_001305968.1:p.Thr61=
NM_001319041.1:c.182C=	NP_001305970.1:p.Thr61=
NM_001319042.1:c.170C=	NP_001305971.1:p.Thr57=
NM_001446.4:c.182C=	NP_001437.1:p.Thr61=
NM_001446.5:c.182C= MANE Select	NP_001437.1:p.Thr61=
NM_001319041.2:c.182C=	NP_001305970.1:p.Thr61=
NM_001319039.2:c.182C=	NP_001305968.1:p.Thr61=
NM_001319042.2:c.170C=	NP_001305971.1:p.Thr57=