Canonical Allele Identifier: CA1595452569
Gene: FABP6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.160235521A= , CM000667.2:g.160235521A= GRCh38
NC_000005.9:g.159662528A= , CM000667.1:g.159662528A= GRCh37
NC_000005.8:g.159595106A= NCBI36
NG_029500.1:g.53155A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000402432.4:c.333+612A= MANE Select ENSP00000385433.4:n.333+612A=
ENST00000393980.8:c.480+612A= ENSP00000377549.4:n.480+612A=
ENST00000402432.3:c.333+612A= ENSP00000385433.3:n.333+612A=
ENST00000521362.1:n.329+612A=
ENST00000523955.5:c.658+612A= ENSP00000428766.1:n.658+612A=
NM_001040442.1:c.480+612A= NP_001035532.1:n.480+612A=
NM_001130958.1:c.480+612A= NP_001124430.1:n.480+612A=
NM_001445.2:c.333+612A= NP_001436.1:n.333+612A=
XM_006714830.2:c.333+612A= XP_006714893.1:n.333+612A=
XM_011534463.1:c.396+612A= XP_011532765.1:n.396+612A=
NM_001130958.2:c.480+612A= NP_001124430.1:n.480+612A=
NM_001445.3:c.333+612A= MANE Select NP_001436.1:n.333+612A=