Canonical Allele Identifier: CA10638886

Gene: FSHB ARL14EP-DT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.30234748T>G , CM000673.2:g.30234748T>G	GRCh38
NC_000011.9:g.30256295T>G , CM000673.1:g.30256295T>G	GRCh37
NC_000011.8:g.30212871T>G	NCBI36
NG_008144.1:g.8733T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254122.8:c.*948T>G (FSHB)	ENSP00000254122.3:n.*948T>G
ENST00000533718.2:c.*948T>G (FSHB) MANE Select	ENSP00000433424.1:n.*948T>G
ENST00000254122.7:c.*948T>G (FSHB)	ENSP00000254122.3:n.*948T>G
ENST00000417547.1:c.*948T>G (FSHB)	ENSP00000416606.1:n.*948T>G
ENST00000533718.1:c.*948T>G (FSHB)	ENSP00000433424.1:n.*948T>G
NM_000510.2:c.*948T>G (FSHB)	NP_000501.1:n.*948T>G
NM_001018080.1:c.*948T>G (FSHB)	NP_001018090.1:n.*948T>G
XR_931152.1:n.463+82142A>C (ARL14EP-DT)
XR_931153.1:n.284+82142A>C (ARL14EP-DT)
XR_931152.2:n.463+82142A>C (ARL14EP-DT)
NM_000510.3:c.*948T>G (FSHB)	NP_000501.1:n.*948T>G
NM_001018080.2:c.*948T>G (FSHB)	NP_001018090.1:n.*948T>G
NM_000510.4:c.*948T>G (FSHB)	NP_000501.1:n.*948T>G
NM_001018080.3:c.*948T>G (FSHB)	NP_001018090.1:n.*948T>G
NM_001382289.1:c.*948T>G (FSHB) MANE Select	NP_001369218.1:n.*948T>G