Canonical Allele Identifier: CA1660115205
Gene: FABP7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.122780224C= , CM000668.2:g.122780224C= GRCh38
NC_000006.11:g.123101369C= , CM000668.1:g.123101369C= GRCh37
NC_000006.10:g.123143068C= NCBI36
NG_050619.1:g.36024C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368444.8:c.74-67C= MANE Select ENSP00000357429.3:n.74-67C=
ENST00000356535.4:c.74-67C= ENSP00000348931.4:n.74-67C=
ENST00000368444.7:c.74-67C= ENSP00000357429.3:n.74-67C=
NM_001446.3:c.74-67C= NP_001437.1:n.74-67C=
XM_005266858.2:c.74-67C= XP_005266915.1:n.74-67C=
NM_001319039.1:c.74-67C= NP_001305968.1:n.74-67C=
NM_001319041.1:c.74-67C= NP_001305970.1:n.74-67C=
NM_001319042.1:c.62-67C= NP_001305971.1:n.62-67C=
NM_001446.4:c.74-67C= NP_001437.1:n.74-67C=
NM_001446.5:c.74-67C= MANE Select NP_001437.1:n.74-67C=
NM_001319041.2:c.74-67C= NP_001305970.1:n.74-67C=
NM_001319039.2:c.74-67C= NP_001305968.1:n.74-67C=
NM_001319042.2:c.62-67C= NP_001305971.1:n.62-67C=