Canonical Allele Identifier: CA2680210785
Gene: FABP7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.122780374_122780412dup , CM000668.2:g.122780374_122780412dup GRCh38
NC_000006.11:g.123101519_123101557dup , CM000668.1:g.123101519_123101557dup GRCh37
NC_000006.10:g.123143218_123143256dup NCBI36
NG_050619.1:g.36174_36212dup

Transcript Alleles

HGVS Amino-acid change
ENST00000368444.8:c.157_195dup MANE Select ENSP00000357429.3:p.Phe65_Gln66insArgThrL...
ENST00000356535.4:c.157_195dup ENSP00000348931.4:p.Phe65_Gln66insArgThrL...
ENST00000368444.7:c.157_195dup ENSP00000357429.3:p.Phe65_Gln66insArgThrL...
NM_001446.3:c.157_195dup NP_001437.1:p.Phe65_Gln66insArgThrLeuSerT...
XM_005266858.2:c.157_195dup XP_005266915.1:p.Phe65_Gln66insArgThrLeuS...
NM_001319039.1:c.157_195dup NP_001305968.1:p.Phe65_Gln66insArgThrLeuS...
NM_001319041.1:c.157_195dup NP_001305970.1:p.Phe65_Gln66insArgThrLeuS...
NM_001319042.1:c.145_183dup NP_001305971.1:p.Phe61_Gln62insArgThrLeuS...
NM_001446.4:c.157_195dup NP_001437.1:p.Phe65_Gln66insArgThrLeuSerT...
NM_001446.5:c.157_195dup MANE Select NP_001437.1:p.Phe65_Gln66insArgThrLeuSerT...
NM_001319041.2:c.157_195dup NP_001305970.1:p.Phe65_Gln66insArgThrLeuS...
NM_001319039.2:c.157_195dup NP_001305968.1:p.Phe65_Gln66insArgThrLeuS...
NM_001319042.2:c.145_183dup NP_001305971.1:p.Phe61_Gln62insArgThrLeuS...