Canonical Allele Identifier: CA374618821

Gene: WHRN

Linked Data

• MyVariant Identifiers: chr9:g.117165078C>T (hg19) ; chr9:g.114402798C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114402798C>T , CM000671.2:g.114402798C>T	GRCh38
NC_000009.11:g.117165078C>T , CM000671.1:g.117165078C>T	GRCh37
NC_000009.10:g.116204899C>T	NCBI36
NG_016700.1:g.107659G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699485.1:c.1024G>A	ENSP00000514396.1:p.Asp342Asn
ENST00000362057.4:c.2680G>A MANE Select	ENSP00000354623.3:p.Asp894Asn
ENST00000674036.8:c.1653G>A
ENST00000674048.1:n.2561G>A
ENST00000265134.10:c.1531G>A	ENSP00000265134.6:p.Asp511Asn
ENST00000362057.3:c.2680G>A	ENSP00000354623.3:p.Asp894Asn
ENST00000374059.7:c.1627G>A	ENSP00000363172.3:p.Asp543Asn
NM_001083885.2:c.1531G>A	NP_001077354.2:p.Asp511Asn
NM_001173425.1:c.2677G>A	NP_001166896.1:p.Asp893Asn
NM_015404.3:c.2680G>A	NP_056219.3:p.Asp894Asn
XM_005251897.3:c.2017G>A	XP_005251954.2:p.Asp673Asn
XM_011518484.1:c.2713G>A	XP_011516786.1:p.Asp905Asn
XM_011518485.1:c.2713G>A	XP_011516787.1:p.Asp905Asn
XM_011518486.1:c.2710G>A	XP_011516788.1:p.Asp904Asn
XM_011518487.1:c.2587G>A	XP_011516789.1:p.Asp863Asn
XM_011518488.1:c.2470G>A	XP_011516790.1:p.Asp824Asn
XM_011518495.1:c.1390G>A	XP_011516797.1:p.Asp464Asn
NM_001346890.1:c.1627G>A	NP_001333819.1:p.Asp543Asn
XM_011518486.2:c.2710G>A	XP_011516788.1:p.Asp904Asn
XM_011518487.2:c.2587G>A	XP_011516789.1:p.Asp863Asn
XM_011518488.2:c.2470G>A	XP_011516790.1:p.Asp824Asn
NM_015404.4:c.2680G>A MANE Select	NP_056219.3:p.Asp894Asn
NM_001173425.2:c.2677G>A	NP_001166896.1:p.Asp893Asn
NM_001083885.3:c.1531G>A	NP_001077354.2:p.Asp511Asn