Canonical Allele Identifier: CA357397049
Gene: FGF5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.81207532T>G (hg19) chr4:g.80286378T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.80286378T>G , CM000666.2:g.80286378T>G GRCh38
NC_000004.11:g.81207532T>G , CM000666.1:g.81207532T>G GRCh37
NC_000004.10:g.81426556T>G NCBI36
NG_029501.1:g.24791T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000312465.12:c.513T>G MANE Select ENSP00000311697.7:p.Tyr171Ter
ENST00000312465.11:c.513T>G ENSP00000311697.7:p.Tyr171Ter
ENST00000456523.3:c.*37T>G ENSP00000398353.3:n.*37T>G
ENST00000503413.1:n.462T>G
ENST00000507780.1:c.342+11366T>G ENSP00000423903.1:n.342+11366T>G
NM_001291812.1:c.84T>G NP_001278741.1:p.Tyr28Ter
NM_004464.3:c.513T>G NP_004455.2:p.Tyr171Ter
NM_033143.2:c.*37T>G NP_149134.1:n.*37T>G
NM_001291812.2:c.84T>G NP_001278741.1:p.Tyr28Ter
NM_004464.4:c.513T>G MANE Select NP_004455.2:p.Tyr171Ter
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Search 100 bp 3'