Canonical Allele Identifier: CA1933232

Gene: FAP

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162174974G>T , CM000664.2:g.162174974G>T	GRCh38
NC_000002.11:g.163031484G>T , CM000664.1:g.163031484G>T	GRCh37
NC_000002.10:g.162739730G>T	NCBI36
NG_027991.1:g.73562C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004460.5:c.1870-8C>A MANE Select	NP_004451.2:n.1870-8C>A
ENST00000188790.9:c.1870-8C>A MANE Select	ENSP00000188790.4:n.1870-8C>A
NM_001291807.1:c.1795-8C>A	NP_001278736.1:n.1795-8C>A
NM_001291807.2:c.1795-8C>A	NP_001278736.1:n.1795-8C>A
NM_001291807.3:c.1795-8C>A	NP_001278736.1:n.1795-8C>A
NM_004460.3:c.1870-8C>A	NP_004451.2:n.1870-8C>A
NM_004460.4:c.1870-8C>A	NP_004451.2:n.1870-8C>A
ENST00000188790.8:c.1870-8C>A	ENSP00000188790.4:n.1870-8C>A
ENST00000422436.5:c.829-8C>A	ENSP00000417028.1:n.829-8C>A
ENST00000443424.5:c.1795-8C>A	ENSP00000411391.1:n.1795-8C>A
ENST00000461506.1:n.171-8C>A
ENST00000480044.5:n.1696C>A
ENST00000627638.2:c.1867-8C>A	ENSP00000485844.1:n.1867-8C>A
XM_011510796.1:c.1840-8C>A	XP_011509098.1:n.1840-8C>A
XM_011510796.3:c.1840-8C>A	XP_011509098.1:n.1840-8C>A