Canonical Allele Identifier: CA11616659

Gene: FGF12

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.192179429G>A , CM000665.2:g.192179429G>A	GRCh38
NC_000003.11:g.191897218G>A , CM000665.1:g.191897218G>A	GRCh37
NC_000003.10:g.193379912G>A	NCBI36
NG_051966.1:g.553171C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454309.7:c.415-8773C>T	ENSP00000413496.2:n.415-8773C>T
ENST00000683451.2:c.229-8773C>T	ENSP00000508366.1:n.229-8773C>T
ENST00000682572.1:n.417-35302C>T
ENST00000683451.1:c.229-8773C>T	ENSP00000508366.1:n.229-8773C>T
ENST00000683935.1:c.229-8773C>T	ENSP00000507098.1:n.229-8773C>T
ENST00000684282.1:c.157-8773C>T	ENSP00000507149.1:n.157-8773C>T
ENST00000684728.1:c.157-8773C>T	ENSP00000506839.1:n.157-8773C>T
ENST00000445105.7:c.229-8773C>T MANE Select	ENSP00000393686.1:n.229-8773C>T
ENST00000418610.1:c.229-8773C>T	ENSP00000395517.1:n.229-8773C>T
ENST00000430714.5:c.118-8773C>T	ENSP00000410125.1:n.118-8773C>T
ENST00000440901.4:n.100-8773C>T
ENST00000445105.6:c.229-8773C>T	ENSP00000393686.1:n.229-8773C>T
ENST00000448795.5:c.157-8773C>T	ENSP00000412904.1:n.157-8773C>T
ENST00000450716.5:c.229-8773C>T	ENSP00000397635.1:n.229-8773C>T
ENST00000454309.6:c.415-8773C>T	ENSP00000413496.2:n.415-8773C>T
NM_004113.5:c.229-8773C>T	NP_004104.3:n.229-8773C>T
NM_021032.4:c.415-8773C>T	NP_066360.1:n.415-8773C>T
XM_005247227.1:c.307-8773C>T	XP_005247284.1:n.307-8773C>T
XM_006713538.2:c.220-8773C>T	XP_006713601.1:n.220-8773C>T
XM_006713539.2:c.157-8773C>T	XP_006713602.1:n.157-8773C>T
XM_005247227.2:c.307-8773C>T	XP_005247284.1:n.307-8773C>T
XM_006713538.3:c.220-8773C>T	XP_006713601.1:n.220-8773C>T
XM_024453395.1:c.157-8773C>T	XP_024309163.1:n.157-8773C>T
NM_001377292.1:c.118-8773C>T	NP_001364221.1:n.118-8773C>T
NM_001377293.1:c.157-8773C>T	NP_001364222.1:n.157-8773C>T
NM_001377294.1:c.157-8773C>T	NP_001364223.1:n.157-8773C>T
NM_004113.6:c.229-8773C>T MANE Select	NP_004104.3:n.229-8773C>T
NM_021032.5:c.415-8773C>T	NP_066360.1:n.415-8773C>T