Canonical Allele Identifier: CA570227179

Gene: FABP7

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.122783162G>A , CM000668.2:g.122783162G>A	GRCh38
NC_000006.11:g.123104307G>A , CM000668.1:g.123104307G>A	GRCh37
NC_000006.10:g.123146006G>A	NCBI36
NG_050619.1:g.38962G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368444.8:c.349-555G>A MANE Select	ENSP00000357429.3:n.349-555G>A
ENST00000368444.7:c.349-555G>A	ENSP00000357429.3:n.349-555G>A
NM_001446.3:c.349-555G>A	NP_001437.1:n.349-555G>A
NM_001319041.1:c.*2651G>A	NP_001305970.1:n.*2651G>A
NM_001319042.1:c.337-555G>A	NP_001305971.1:n.337-555G>A
NM_001446.4:c.349-555G>A	NP_001437.1:n.349-555G>A
NM_001446.5:c.349-555G>A MANE Select	NP_001437.1:n.349-555G>A
NM_001319041.2:c.*2651G>A	NP_001305970.1:n.*2651G>A
NM_001319042.2:c.337-555G>A	NP_001305971.1:n.337-555G>A