Canonical Allele Identifier: CA2838522002

Gene: FGF12

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.192144338A>G , CM000665.2:g.192144338A>G	GRCh38
NC_000003.11:g.191862127A>G , CM000665.1:g.191862127A>G	GRCh37
NC_000003.10:g.193344821A>G	NCBI36
NG_051966.1:g.588262T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454309.7:c.614-211T>C	ENSP00000413496.2:n.614-211T>C
ENST00000683451.2:c.428-211T>C	ENSP00000508366.1:n.428-211T>C
ENST00000682572.1:n.417-211T>C
ENST00000683451.1:c.428-211T>C	ENSP00000508366.1:n.428-211T>C
ENST00000683935.1:c.428-211T>C	ENSP00000507098.1:n.428-211T>C
ENST00000684282.1:c.356-211T>C	ENSP00000507149.1:n.356-211T>C
ENST00000684728.1:c.356-211T>C	ENSP00000506839.1:n.356-211T>C
ENST00000445105.7:c.428-211T>C MANE Select	ENSP00000393686.1:n.428-211T>C
ENST00000430714.5:c.317-211T>C	ENSP00000410125.1:n.317-211T>C
ENST00000440901.4:n.299-211T>C
ENST00000445105.6:c.428-211T>C	ENSP00000393686.1:n.428-211T>C
ENST00000448795.5:c.356-211T>C	ENSP00000412904.1:n.356-211T>C
ENST00000450716.5:c.428-211T>C	ENSP00000397635.1:n.428-211T>C
ENST00000454309.6:c.614-211T>C	ENSP00000413496.2:n.614-211T>C
NM_004113.5:c.428-211T>C	NP_004104.3:n.428-211T>C
NM_021032.4:c.614-211T>C	NP_066360.1:n.614-211T>C
XM_005247227.1:c.506-211T>C	XP_005247284.1:n.506-211T>C
XM_006713538.2:c.419-211T>C	XP_006713601.1:n.419-211T>C
XM_006713539.2:c.356-211T>C	XP_006713602.1:n.356-211T>C
XM_005247227.2:c.506-211T>C	XP_005247284.1:n.506-211T>C
XM_006713538.3:c.419-211T>C	XP_006713601.1:n.419-211T>C
XM_024453395.1:c.356-211T>C	XP_024309163.1:n.356-211T>C
NM_001377292.1:c.317-211T>C	NP_001364221.1:n.317-211T>C
NM_001377293.1:c.356-211T>C	NP_001364222.1:n.356-211T>C
NM_001377294.1:c.356-211T>C	NP_001364223.1:n.356-211T>C
NM_004113.6:c.428-211T>C MANE Select	NP_004104.3:n.428-211T>C
NM_021032.5:c.614-211T>C	NP_066360.1:n.614-211T>C