Canonical Allele Identifier: CA355866479

Gene: FGF12

Linked Data

• MyVariant Identifiers: chr3:g.192053235G>C (hg19) ; chr3:g.192335446G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.192335446G>C , CM000665.2:g.192335446G>C	GRCh38
NC_000003.11:g.192053235G>C , CM000665.1:g.192053235G>C	GRCh37
NC_000003.10:g.193535929G>C	NCBI36
NG_051966.1:g.397154C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000454309.7:c.329C>G	ENSP00000413496.2:p.Pro110Arg
ENST00000682819.2:n.396C>G
ENST00000683451.2:c.143C>G	ENSP00000508366.1:p.Pro48Arg
ENST00000682572.1:n.331C>G
ENST00000682819.1:n.362C>G
ENST00000683451.1:c.143C>G	ENSP00000508366.1:p.Pro48Arg
ENST00000683935.1:c.143C>G	ENSP00000507098.1:p.Pro48Arg
ENST00000684282.1:c.71C>G	ENSP00000507149.1:p.Pro24Arg
ENST00000684728.1:c.71C>G	ENSP00000506839.1:p.Pro24Arg
ENST00000445105.7:c.143C>G MANE Select	ENSP00000393686.1:p.Pro48Arg
ENST00000418610.1:c.143C>G	ENSP00000395517.1:p.Pro48Arg
ENST00000430714.5:c.32C>G	ENSP00000410125.1:p.Pro11Arg
ENST00000445105.6:c.143C>G	ENSP00000393686.1:p.Pro48Arg
ENST00000448795.5:c.71C>G	ENSP00000412904.1:p.Pro24Arg
ENST00000450716.5:c.143C>G	ENSP00000397635.1:p.Pro48Arg
ENST00000454309.6:c.329C>G	ENSP00000413496.2:p.Pro110Arg
NM_004113.5:c.143C>G	NP_004104.3:p.Pro48Arg
NM_021032.4:c.329C>G	NP_066360.1:p.Pro110Arg
XM_005247227.1:c.221C>G	XP_005247284.1:p.Pro74Arg
XM_006713538.2:c.134C>G	XP_006713601.1:p.Pro45Arg
XM_006713539.2:c.71C>G	XP_006713602.1:p.Pro24Arg
XM_005247227.2:c.221C>G	XP_005247284.1:p.Pro74Arg
XM_006713538.3:c.134C>G	XP_006713601.1:p.Pro45Arg
XM_024453395.1:c.71C>G	XP_024309163.1:p.Pro24Arg
NM_001377292.1:c.32C>G	NP_001364221.1:p.Pro11Arg
NM_001377293.1:c.71C>G	NP_001364222.1:p.Pro24Arg
NM_001377294.1:c.71C>G	NP_001364223.1:p.Pro24Arg
NM_004113.6:c.143C>G MANE Select	NP_004104.3:p.Pro48Arg
NM_021032.5:c.329C>G	NP_066360.1:p.Pro110Arg