Canonical Allele Identifier: CA1797460532

Gene: FABP12

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.81532989C= , CM000670.2:g.81532989C=	GRCh38
NC_000008.10:g.82445224C= , CM000670.1:g.82445224C=	GRCh37
NC_000008.9:g.82607779C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360464.6:c.-76+813G= MANE Select	ENSP00000353650.4:n.-76+813G=
ENST00000360464.5:c.-76+813G=	ENSP00000353650.4:n.-76+813G=
ENST00000692030.1:c.-58-1616G=	ENSP00000510293.1:n.-58-1616G=
XM_005251285.3:c.-76+813G=	XP_005251342.1:n.-76+813G=
XM_006716465.2:c.-59+813G=	XP_006716528.1:n.-59+813G=
XM_011517575.1:c.-75-1599G=	XP_011515877.1:n.-75-1599G=
XM_011517576.1:c.-76+94G=	XP_011515878.1:n.-76+94G=
XM_011517577.1:c.-58-1616G=	XP_011515879.1:n.-58-1616G=
XR_242492.2:n.556+6533C=
NM_001105281.2:c.-76+813G=	NP_001098751.1:n.-76+813G=
XM_006716465.3:c.-59+813G=	XP_006716528.1:n.-59+813G=
XM_011517577.2:c.-58-1616G=	XP_011515879.1:n.-58-1616G=
XR_001745980.1:n.819+6533C=
XR_242492.3:n.567+6533C=
NM_001105281.4:c.-76+813G=	NP_001098751.1:n.-76+813G=
NM_001105281.5:c.-76+813G=	NP_001098751.1:n.-76+813G=