Canonical Allele Identifier: CA1873825292

Gene: WHRN

Linked Data

• dbSNP Id: rs1465322169

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114402695G>C , CM000671.2:g.114402695G>C	GRCh38
NC_000009.11:g.117164975G>C , CM000671.1:g.117164975G>C	GRCh37
NC_000009.10:g.116204796G>C	NCBI36
NG_016700.1:g.107762C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699485.1:c.1127C>G	ENSP00000514396.1:n.1127C>G
ENST00000362057.4:c.*59C>G MANE Select	ENSP00000354623.3:n.*59C>G
ENST00000674036.8:c.1756C>G
ENST00000674048.1:n.2664C>G
ENST00000265134.10:c.*59C>G	ENSP00000265134.6:n.*59C>G
ENST00000362057.3:c.*59C>G	ENSP00000354623.3:n.*59C>G
ENST00000374059.7:c.*59C>G	ENSP00000363172.3:n.*59C>G
NM_001083885.2:c.*59C>G	NP_001077354.2:n.*59C>G
NM_001173425.1:c.*59C>G	NP_001166896.1:n.*59C>G
NM_015404.3:c.*59C>G	NP_056219.3:n.*59C>G
XM_005251897.3:c.*59C>G	XP_005251954.2:n.*59C>G
XM_011518484.1:c.*59C>G	XP_011516786.1:n.*59C>G
XM_011518485.1:c.*59C>G	XP_011516787.1:n.*59C>G
XM_011518486.1:c.*59C>G	XP_011516788.1:n.*59C>G
XM_011518487.1:c.*59C>G	XP_011516789.1:n.*59C>G
XM_011518488.1:c.*59C>G	XP_011516790.1:n.*59C>G
XM_011518495.1:c.*59C>G	XP_011516797.1:n.*59C>G
NM_001346890.1:c.*59C>G	NP_001333819.1:n.*59C>G
XM_011518486.2:c.*59C>G	XP_011516788.1:n.*59C>G
XM_011518487.2:c.*59C>G	XP_011516789.1:n.*59C>G
XM_011518488.2:c.*59C>G	XP_011516790.1:n.*59C>G
NM_015404.4:c.*59C>G MANE Select	NP_056219.3:n.*59C>G
NM_001173425.2:c.*59C>G	NP_001166896.1:n.*59C>G
NM_001083885.3:c.*59C>G	NP_001077354.2:n.*59C>G