Canonical Allele Identifier: CA1660115294

Gene: FABP7

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.122780416C= , CM000668.2:g.122780416C=	GRCh38
NC_000006.11:g.123101561C= , CM000668.1:g.123101561C=	GRCh37
NC_000006.10:g.123143260C=	NCBI36
NG_050619.1:g.36216C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000368444.8:c.199C= MANE Select	ENSP00000357429.3:p.Leu67=
ENST00000356535.4:c.199C=	ENSP00000348931.4:p.Leu67=
ENST00000368444.7:c.199C=	ENSP00000357429.3:p.Leu67=
NM_001446.3:c.199C=	NP_001437.1:p.Leu67=
XM_005266858.2:c.199C=	XP_005266915.1:p.Leu67=
NM_001319039.1:c.199C=	NP_001305968.1:p.Leu67=
NM_001319041.1:c.199C=	NP_001305970.1:p.Leu67=
NM_001319042.1:c.187C=	NP_001305971.1:p.Leu63=
NM_001446.4:c.199C=	NP_001437.1:p.Leu67=
NM_001446.5:c.199C= MANE Select	NP_001437.1:p.Leu67=
NM_001319041.2:c.199C=	NP_001305970.1:p.Leu67=
NM_001319039.2:c.199C=	NP_001305968.1:p.Leu67=
NM_001319042.2:c.187C=	NP_001305971.1:p.Leu63=