Canonical Allele Identifier: CA466910911

Gene: WHRN

Linked Data

• MyVariant Identifiers: chr9:g.117165157C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114402877C>T , CM000671.2:g.114402877C>T	GRCh38
NC_000009.11:g.117165157C>T , CM000671.1:g.117165157C>T	GRCh37
NC_000009.10:g.116204978C>T	NCBI36
NG_016700.1:g.107580G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699485.1:c.945G>A	ENSP00000514396.1:p.Val315=
ENST00000362057.4:c.2601G>A MANE Select	ENSP00000354623.3:p.Val867=
ENST00000674036.8:c.1574G>A
ENST00000674048.1:n.2482G>A
ENST00000265134.10:c.1452G>A	ENSP00000265134.6:p.Val484=
ENST00000362057.3:c.2601G>A	ENSP00000354623.3:p.Val867=
ENST00000374059.7:c.1548G>A	ENSP00000363172.3:p.Val516=
NM_001083885.2:c.1452G>A	NP_001077354.2:p.Val484=
NM_001173425.1:c.2598G>A	NP_001166896.1:p.Val866=
NM_015404.3:c.2601G>A	NP_056219.3:p.Val867=
XM_005251897.3:c.1938G>A	XP_005251954.2:p.Val646=
XM_011518484.1:c.2634G>A	XP_011516786.1:p.Val878=
XM_011518485.1:c.2634G>A	XP_011516787.1:p.Val878=
XM_011518486.1:c.2631G>A	XP_011516788.1:p.Val877=
XM_011518487.1:c.2508G>A	XP_011516789.1:p.Val836=
XM_011518488.1:c.2391G>A	XP_011516790.1:p.Val797=
XM_011518495.1:c.1311G>A	XP_011516797.1:p.Val437=
NM_001346890.1:c.1548G>A	NP_001333819.1:p.Val516=
XM_011518486.2:c.2631G>A	XP_011516788.1:p.Val877=
XM_011518487.2:c.2508G>A	XP_011516789.1:p.Val836=
XM_011518488.2:c.2391G>A	XP_011516790.1:p.Val797=
NM_015404.4:c.2601G>A MANE Select	NP_056219.3:p.Val867=
NM_001173425.2:c.2598G>A	NP_001166896.1:p.Val866=
NM_001083885.3:c.1452G>A	NP_001077354.2:p.Val484=