Canonical Allele Identifier: CA374619071

Gene: WHRN

Linked Data

• MyVariant Identifiers: chr9:g.117165201G>T (hg19) ; chr9:g.114402921G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114402921G>T , CM000671.2:g.114402921G>T	GRCh38
NC_000009.11:g.117165201G>T , CM000671.1:g.117165201G>T	GRCh37
NC_000009.10:g.116205022G>T	NCBI36
NG_016700.1:g.107536C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699485.1:c.901C>A	ENSP00000514396.1:p.His301Asn
ENST00000362057.4:c.2557C>A MANE Select	ENSP00000354623.3:p.His853Asn
ENST00000674036.8:c.1530C>A
ENST00000674048.1:n.2438C>A
ENST00000265134.10:c.1408C>A	ENSP00000265134.6:p.His470Asn
ENST00000362057.3:c.2557C>A	ENSP00000354623.3:p.His853Asn
ENST00000374059.7:c.1504C>A	ENSP00000363172.3:p.His502Asn
NM_001083885.2:c.1408C>A	NP_001077354.2:p.His470Asn
NM_001173425.1:c.2554C>A	NP_001166896.1:p.His852Asn
NM_015404.3:c.2557C>A	NP_056219.3:p.His853Asn
XM_005251897.3:c.1894C>A	XP_005251954.2:p.His632Asn
XM_011518484.1:c.2590C>A	XP_011516786.1:p.His864Asn
XM_011518485.1:c.2590C>A	XP_011516787.1:p.His864Asn
XM_011518486.1:c.2587C>A	XP_011516788.1:p.His863Asn
XM_011518487.1:c.2464C>A	XP_011516789.1:p.His822Asn
XM_011518488.1:c.2347C>A	XP_011516790.1:p.His783Asn
XM_011518495.1:c.1267C>A	XP_011516797.1:p.His423Asn
XR_929747.1:n.3494C>A
XR_929748.1:n.3392C>A
NM_001346890.1:c.1504C>A	NP_001333819.1:p.His502Asn
XM_011518486.2:c.2587C>A	XP_011516788.1:p.His863Asn
XM_011518487.2:c.2464C>A	XP_011516789.1:p.His822Asn
XM_011518488.2:c.2347C>A	XP_011516790.1:p.His783Asn
XR_929747.2:n.2805C>A
XR_929748.2:n.2703C>A
NM_015404.4:c.2557C>A MANE Select	NP_056219.3:p.His853Asn
NM_001173425.2:c.2554C>A	NP_001166896.1:p.His852Asn
NM_001083885.3:c.1408C>A	NP_001077354.2:p.His470Asn