Canonical Allele Identifier: CA374618929

Gene: WHRN

Linked Data

• MyVariant Identifiers: chr9:g.117165132C>G (hg19) ; chr9:g.114402852C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114402852C>G , CM000671.2:g.114402852C>G	GRCh38
NC_000009.11:g.117165132C>G , CM000671.1:g.117165132C>G	GRCh37
NC_000009.10:g.116204953C>G	NCBI36
NG_016700.1:g.107605G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699485.1:c.970G>C	ENSP00000514396.1:p.Glu324Gln
ENST00000362057.4:c.2626G>C MANE Select	ENSP00000354623.3:p.Glu876Gln
ENST00000674036.8:c.1599G>C
ENST00000674048.1:n.2507G>C
ENST00000265134.10:c.1477G>C	ENSP00000265134.6:p.Glu493Gln
ENST00000362057.3:c.2626G>C	ENSP00000354623.3:p.Glu876Gln
ENST00000374059.7:c.1573G>C	ENSP00000363172.3:p.Glu525Gln
NM_001083885.2:c.1477G>C	NP_001077354.2:p.Glu493Gln
NM_001173425.1:c.2623G>C	NP_001166896.1:p.Glu875Gln
NM_015404.3:c.2626G>C	NP_056219.3:p.Glu876Gln
XM_005251897.3:c.1963G>C	XP_005251954.2:p.Glu655Gln
XM_011518484.1:c.2659G>C	XP_011516786.1:p.Glu887Gln
XM_011518485.1:c.2659G>C	XP_011516787.1:p.Glu887Gln
XM_011518486.1:c.2656G>C	XP_011516788.1:p.Glu886Gln
XM_011518487.1:c.2533G>C	XP_011516789.1:p.Glu845Gln
XM_011518488.1:c.2416G>C	XP_011516790.1:p.Glu806Gln
XM_011518495.1:c.1336G>C	XP_011516797.1:p.Glu446Gln
NM_001346890.1:c.1573G>C	NP_001333819.1:p.Glu525Gln
XM_011518486.2:c.2656G>C	XP_011516788.1:p.Glu886Gln
XM_011518487.2:c.2533G>C	XP_011516789.1:p.Glu845Gln
XM_011518488.2:c.2416G>C	XP_011516790.1:p.Glu806Gln
NM_015404.4:c.2626G>C MANE Select	NP_056219.3:p.Glu876Gln
NM_001173425.2:c.2623G>C	NP_001166896.1:p.Glu875Gln
NM_001083885.3:c.1477G>C	NP_001077354.2:p.Glu493Gln