Canonical Allele Identifier: CA374618722

Gene: WHRN

Linked Data

• MyVariant Identifiers: chr9:g.117165034C>A (hg19) ; chr9:g.114402754C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114402754C>A , CM000671.2:g.114402754C>A	GRCh38
NC_000009.11:g.117165034C>A , CM000671.1:g.117165034C>A	GRCh37
NC_000009.10:g.116204855C>A	NCBI36
NG_016700.1:g.107703G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000699485.1:c.1068G>T	ENSP00000514396.1:p.Ter356Tyr
ENST00000362057.4:c.2724G>T MANE Select	ENSP00000354623.3:p.Ter908Tyr
ENST00000674036.8:c.1697G>T
ENST00000674048.1:n.2605G>T
ENST00000265134.10:c.1575G>T	ENSP00000265134.6:p.Ter525Tyr
ENST00000362057.3:c.2724G>T	ENSP00000354623.3:p.Ter908Tyr
ENST00000374059.7:c.1671G>T	ENSP00000363172.3:p.Ter557Tyr
NM_001083885.2:c.1575G>T	NP_001077354.2:p.Ter525Tyr
NM_001173425.1:c.2721G>T	NP_001166896.1:p.Ter907Tyr
NM_015404.3:c.2724G>T	NP_056219.3:p.Ter908Tyr
XM_005251897.3:c.2061G>T	XP_005251954.2:p.Ter687Tyr
XM_011518484.1:c.2757G>T	XP_011516786.1:p.Ter919Tyr
XM_011518485.1:c.2757G>T	XP_011516787.1:p.Ter919Tyr
XM_011518486.1:c.2754G>T	XP_011516788.1:p.Ter918Tyr
XM_011518487.1:c.2631G>T	XP_011516789.1:p.Ter877Tyr
XM_011518488.1:c.2514G>T	XP_011516790.1:p.Ter838Tyr
XM_011518495.1:c.1434G>T	XP_011516797.1:p.Ter478Tyr
NM_001346890.1:c.1671G>T	NP_001333819.1:p.Ter557Tyr
XM_011518486.2:c.2754G>T	XP_011516788.1:p.Ter918Tyr
XM_011518487.2:c.2631G>T	XP_011516789.1:p.Ter877Tyr
XM_011518488.2:c.2514G>T	XP_011516790.1:p.Ter838Tyr
NM_015404.4:c.2724G>T MANE Select	NP_056219.3:p.Ter908Tyr
NM_001173425.2:c.2721G>T	NP_001166896.1:p.Ter907Tyr
NM_001083885.3:c.1575G>T	NP_001077354.2:p.Ter525Tyr