Canonical Allele Identifier: CA2612909752

Gene: FSHB ARL14EP-DT

Linked Data

• gnomAD v4: 11-30233550-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.30233550T>C , CM000673.2:g.30233550T>C	GRCh38
NC_000011.9:g.30255097T>C , CM000673.1:g.30255097T>C	GRCh37
NC_000011.8:g.30211673T>C	NCBI36
NG_008144.1:g.7535T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254122.8:c.160-20T>C (FSHB)	ENSP00000254122.3:n.160-20T>C
ENST00000533718.2:c.160-20T>C (FSHB) MANE Select	ENSP00000433424.1:n.160-20T>C
ENST00000254122.7:c.160-20T>C (FSHB)	ENSP00000254122.3:n.160-20T>C
ENST00000417547.1:c.160-20T>C (FSHB)	ENSP00000416606.1:n.160-20T>C
ENST00000533718.1:c.160-20T>C (FSHB)	ENSP00000433424.1:n.160-20T>C
NM_000510.2:c.160-20T>C (FSHB)	NP_000501.1:n.160-20T>C
NM_001018080.1:c.160-20T>C (FSHB)	NP_001018090.1:n.160-20T>C
XM_011519964.1:c.160-20T>C (FSHB)	XP_011518266.1:n.160-20T>C
XR_931152.1:n.463+83340A>G (ARL14EP-DT)
XR_931153.1:n.284+83340A>G (ARL14EP-DT)
XR_931152.2:n.463+83340A>G (ARL14EP-DT)
NM_000510.3:c.160-20T>C (FSHB)	NP_000501.1:n.160-20T>C
NM_001018080.2:c.160-20T>C (FSHB)	NP_001018090.1:n.160-20T>C
NM_000510.4:c.160-20T>C (FSHB)	NP_000501.1:n.160-20T>C
NM_001018080.3:c.160-20T>C (FSHB)	NP_001018090.1:n.160-20T>C
NM_001382289.1:c.160-20T>C (FSHB) MANE Select	NP_001369218.1:n.160-20T>C