Canonical Allele Identifier: CA11489930
Gene: FGF12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.192195081C>T , CM000665.2:g.192195081C>T GRCh38
NC_000003.11:g.191912870C>T , CM000665.1:g.191912870C>T GRCh37
NC_000003.10:g.193395564C>T NCBI36
NG_051966.1:g.537519G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000454309.7:c.415-24425G>A ENSP00000413496.2:n.415-24425G>A
ENST00000683451.2:c.229-24425G>A ENSP00000508366.1:n.229-24425G>A
ENST00000682572.1:n.417-50954G>A
ENST00000683451.1:c.229-24425G>A ENSP00000508366.1:n.229-24425G>A
ENST00000683935.1:c.229-24425G>A ENSP00000507098.1:n.229-24425G>A
ENST00000684282.1:c.157-24425G>A ENSP00000507149.1:n.157-24425G>A
ENST00000684728.1:c.157-24425G>A ENSP00000506839.1:n.157-24425G>A
ENST00000445105.7:c.229-24425G>A MANE Select ENSP00000393686.1:n.229-24425G>A
ENST00000418610.1:c.229-24425G>A ENSP00000395517.1:n.229-24425G>A
ENST00000430714.5:c.118-24425G>A ENSP00000410125.1:n.118-24425G>A
ENST00000440901.4:n.100-24425G>A
ENST00000445105.6:c.229-24425G>A ENSP00000393686.1:n.229-24425G>A
ENST00000448795.5:c.157-24425G>A ENSP00000412904.1:n.157-24425G>A
ENST00000450716.5:c.229-24425G>A ENSP00000397635.1:n.229-24425G>A
ENST00000454309.6:c.415-24425G>A ENSP00000413496.2:n.415-24425G>A
NM_004113.5:c.229-24425G>A NP_004104.3:n.229-24425G>A
NM_021032.4:c.415-24425G>A NP_066360.1:n.415-24425G>A
XM_005247227.1:c.307-24425G>A XP_005247284.1:n.307-24425G>A
XM_006713538.2:c.220-24425G>A XP_006713601.1:n.220-24425G>A
XM_006713539.2:c.157-24425G>A XP_006713602.1:n.157-24425G>A
XM_005247227.2:c.307-24425G>A XP_005247284.1:n.307-24425G>A
XM_006713538.3:c.220-24425G>A XP_006713601.1:n.220-24425G>A
XM_024453395.1:c.157-24425G>A XP_024309163.1:n.157-24425G>A
NM_001377292.1:c.118-24425G>A NP_001364221.1:n.118-24425G>A
NM_001377293.1:c.157-24425G>A NP_001364222.1:n.157-24425G>A
NM_001377294.1:c.157-24425G>A NP_001364223.1:n.157-24425G>A
NM_004113.6:c.229-24425G>A MANE Select NP_004104.3:n.229-24425G>A
NM_021032.5:c.415-24425G>A NP_066360.1:n.415-24425G>A