Canonical Allele Identifier: CA2671179875

Gene: FGF5

Linked Data

• gnomAD v4: 4-80286691-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80286691G>A , CM000666.2:g.80286691G>A	GRCh38
NC_000004.11:g.81207845G>A , CM000666.1:g.81207845G>A	GRCh37
NC_000004.10:g.81426869G>A	NCBI36
NG_029501.1:g.25104G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312465.12:c.*19G>A MANE Select	ENSP00000311697.7:n.*19G>A
ENST00000312465.11:c.*19G>A	ENSP00000311697.7:n.*19G>A
ENST00000456523.3:c.*350G>A	ENSP00000398353.3:n.*350G>A
ENST00000503413.1:n.775G>A
ENST00000507780.1:c.342+11679G>A	ENSP00000423903.1:n.342+11679G>A
NM_001291812.1:c.*19G>A	NP_001278741.1:n.*19G>A
NM_004464.3:c.*19G>A	NP_004455.2:n.*19G>A
NM_033143.2:c.*350G>A	NP_149134.1:n.*350G>A
NM_001291812.2:c.*19G>A	NP_001278741.1:n.*19G>A
NM_004464.4:c.*19G>A MANE Select	NP_004455.2:n.*19G>A