Canonical Allele Identifier: CA2772886460
Gene: FABP7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.122780211del , CM000668.2:g.122780211del GRCh38
NC_000006.11:g.123101356del , CM000668.1:g.123101356del GRCh37
NC_000006.10:g.123143055del NCBI36
NG_050619.1:g.36011del

Transcript Alleles

HGVS Amino-acid change
ENST00000368444.8:c.74-80del MANE Select ENSP00000357429.3:n.74-80del
ENST00000356535.4:c.74-80del ENSP00000348931.4:n.74-80del
ENST00000368444.7:c.74-80del ENSP00000357429.3:n.74-80del
NM_001446.3:c.74-80del NP_001437.1:n.74-80del
XM_005266858.2:c.74-80del XP_005266915.1:n.74-80del
NM_001319039.1:c.74-80del NP_001305968.1:n.74-80del
NM_001319041.1:c.74-80del NP_001305970.1:n.74-80del
NM_001319042.1:c.62-80del NP_001305971.1:n.62-80del
NM_001446.4:c.74-80del NP_001437.1:n.74-80del
NM_001446.5:c.74-80del MANE Select NP_001437.1:n.74-80del
NM_001319041.2:c.74-80del NP_001305970.1:n.74-80del
NM_001319039.2:c.74-80del NP_001305968.1:n.74-80del
NM_001319042.2:c.62-80del NP_001305971.1:n.62-80del
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