Canonical Allele Identifier: CA466910826

Gene: WHRN

Linked Data

• MyVariant Identifiers: chr9:g.117165112G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114402832G>T , CM000671.2:g.114402832G>T	GRCh38
NC_000009.11:g.117165112G>T , CM000671.1:g.117165112G>T	GRCh37
NC_000009.10:g.116204933G>T	NCBI36
NG_016700.1:g.107625C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699485.1:c.990C>A	ENSP00000514396.1:p.Arg330=
ENST00000362057.4:c.2646C>A MANE Select	ENSP00000354623.3:p.Arg882=
ENST00000674036.8:c.1619C>A
ENST00000674048.1:n.2527C>A
ENST00000265134.10:c.1497C>A	ENSP00000265134.6:p.Arg499=
ENST00000362057.3:c.2646C>A	ENSP00000354623.3:p.Arg882=
ENST00000374059.7:c.1593C>A	ENSP00000363172.3:p.Arg531=
NM_001083885.2:c.1497C>A	NP_001077354.2:p.Arg499=
NM_001173425.1:c.2643C>A	NP_001166896.1:p.Arg881=
NM_015404.3:c.2646C>A	NP_056219.3:p.Arg882=
XM_005251897.3:c.1983C>A	XP_005251954.2:p.Arg661=
XM_011518484.1:c.2679C>A	XP_011516786.1:p.Arg893=
XM_011518485.1:c.2679C>A	XP_011516787.1:p.Arg893=
XM_011518486.1:c.2676C>A	XP_011516788.1:p.Arg892=
XM_011518487.1:c.2553C>A	XP_011516789.1:p.Arg851=
XM_011518488.1:c.2436C>A	XP_011516790.1:p.Arg812=
XM_011518495.1:c.1356C>A	XP_011516797.1:p.Arg452=
NM_001346890.1:c.1593C>A	NP_001333819.1:p.Arg531=
XM_011518486.2:c.2676C>A	XP_011516788.1:p.Arg892=
XM_011518487.2:c.2553C>A	XP_011516789.1:p.Arg851=
XM_011518488.2:c.2436C>A	XP_011516790.1:p.Arg812=
NM_015404.4:c.2646C>A MANE Select	NP_056219.3:p.Arg882=
NM_001173425.2:c.2643C>A	NP_001166896.1:p.Arg881=
NM_001083885.3:c.1497C>A	NP_001077354.2:p.Arg499=