Canonical Allele Identifier: CA1595452571
Gene: FABP6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.160235538G= , CM000667.2:g.160235538G= GRCh38
NC_000005.9:g.159662545G= , CM000667.1:g.159662545G= GRCh37
NC_000005.8:g.159595123G= NCBI36
NG_029500.1:g.53172G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000402432.4:c.333+629G= MANE Select ENSP00000385433.4:n.333+629G=
ENST00000393980.8:c.480+629G= ENSP00000377549.4:n.480+629G=
ENST00000402432.3:c.333+629G= ENSP00000385433.3:n.333+629G=
ENST00000521362.1:n.329+629G=
ENST00000523955.5:c.658+629G= ENSP00000428766.1:n.658+629G=
NM_001040442.1:c.480+629G= NP_001035532.1:n.480+629G=
NM_001130958.1:c.480+629G= NP_001124430.1:n.480+629G=
NM_001445.2:c.333+629G= NP_001436.1:n.333+629G=
XM_006714830.2:c.333+629G= XP_006714893.1:n.333+629G=
XM_011534463.1:c.396+629G= XP_011532765.1:n.396+629G=
NM_001130958.2:c.480+629G= NP_001124430.1:n.480+629G=
NM_001445.3:c.333+629G= MANE Select NP_001436.1:n.333+629G=