Canonical Allele Identifier: CA374619947

Gene: WHRN

Linked Data

• MyVariant Identifiers: chr9:g.117166328T>C (hg19) ; chr9:g.114404048T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114404048T>C , CM000671.2:g.114404048T>C	GRCh38
NC_000009.11:g.117166328T>C , CM000671.1:g.117166328T>C	GRCh37
NC_000009.10:g.116206149T>C	NCBI36
NG_016700.1:g.106409A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699485.1:c.610A>G	ENSP00000514396.1:p.Ser204Gly
ENST00000362057.4:c.2266A>G MANE Select	ENSP00000354623.3:p.Ser756Gly
ENST00000674036.8:c.1239A>G
ENST00000674048.1:n.2147A>G
ENST00000265134.10:c.1117A>G	ENSP00000265134.6:p.Ser373Gly
ENST00000362057.3:c.2266A>G	ENSP00000354623.3:p.Ser756Gly
ENST00000374059.7:c.1213A>G	ENSP00000363172.3:p.Ser405Gly
NM_001083885.2:c.1117A>G	NP_001077354.2:p.Ser373Gly
NM_001173425.1:c.2263A>G	NP_001166896.1:p.Ser755Gly
NM_015404.3:c.2266A>G	NP_056219.3:p.Ser756Gly
XM_005251897.3:c.1603A>G	XP_005251954.2:p.Ser535Gly
XM_011518484.1:c.2299A>G	XP_011516786.1:p.Ser767Gly
XM_011518485.1:c.2299A>G	XP_011516787.1:p.Ser767Gly
XM_011518486.1:c.2296A>G	XP_011516788.1:p.Ser766Gly
XM_011518487.1:c.2173A>G	XP_011516789.1:p.Ser725Gly
XM_011518488.1:c.2056A>G	XP_011516790.1:p.Ser686Gly
XM_011518495.1:c.976A>G	XP_011516797.1:p.Ser326Gly
XR_929747.1:n.3203A>G
XR_929748.1:n.3101A>G
NM_001346890.1:c.1213A>G	NP_001333819.1:p.Ser405Gly
XM_011518486.2:c.2296A>G	XP_011516788.1:p.Ser766Gly
XM_011518487.2:c.2173A>G	XP_011516789.1:p.Ser725Gly
XM_011518488.2:c.2056A>G	XP_011516790.1:p.Ser686Gly
XR_929747.2:n.2514A>G
XR_929748.2:n.2412A>G
NM_015404.4:c.2266A>G MANE Select	NP_056219.3:p.Ser756Gly
NM_001173425.2:c.2263A>G	NP_001166896.1:p.Ser755Gly
NM_001083885.3:c.1117A>G	NP_001077354.2:p.Ser373Gly