Canonical Allele Identifier: CA466911632

Gene: WHRN

Linked Data

• gnomAD v4: 9-114406503-G-A
• MyVariant Identifiers: chr9:g.117168783G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114406503G>A , CM000671.2:g.114406503G>A	GRCh38
NC_000009.11:g.117168783G>A , CM000671.1:g.117168783G>A	GRCh37
NC_000009.10:g.116208604G>A	NCBI36
NG_016700.1:g.103954C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000699485.1:c.432C>T	ENSP00000514396.1:p.Ala144=
ENST00000362057.4:c.2088C>T MANE Select	ENSP00000354623.3:p.Ala696=
ENST00000674036.8:c.1061C>T
ENST00000674048.1:n.1969C>T
ENST00000265134.10:c.939C>T	ENSP00000265134.6:p.Ala313=
ENST00000362057.3:c.2088C>T	ENSP00000354623.3:p.Ala696=
ENST00000374059.7:c.1035C>T	ENSP00000363172.3:p.Ala345=
NM_001083885.2:c.939C>T	NP_001077354.2:p.Ala313=
NM_001173425.1:c.2088C>T	NP_001166896.1:p.Ala696=
NM_015404.3:c.2088C>T	NP_056219.3:p.Ala696=
XM_005251897.3:c.1425C>T	XP_005251954.2:p.Ala475=
XM_011518484.1:c.2121C>T	XP_011516786.1:p.Ala707=
XM_011518485.1:c.2121C>T	XP_011516787.1:p.Ala707=
XM_011518486.1:c.2121C>T	XP_011516788.1:p.Ala707=
XM_011518487.1:c.1995C>T	XP_011516789.1:p.Ala665=
XM_011518488.1:c.1878C>T	XP_011516790.1:p.Ala626=
XM_011518495.1:c.798C>T	XP_011516797.1:p.Ala266=
XR_929747.1:n.3025C>T
XR_929748.1:n.2923C>T
NM_001346890.1:c.1035C>T	NP_001333819.1:p.Ala345=
XM_011518486.2:c.2121C>T	XP_011516788.1:p.Ala707=
XM_011518487.2:c.1995C>T	XP_011516789.1:p.Ala665=
XM_011518488.2:c.1878C>T	XP_011516790.1:p.Ala626=
XR_929747.2:n.2336C>T
XR_929748.2:n.2234C>T
NM_015404.4:c.2088C>T MANE Select	NP_056219.3:p.Ala696=
NM_001173425.2:c.2088C>T	NP_001166896.1:p.Ala696=
NM_001083885.3:c.939C>T	NP_001077354.2:p.Ala313=