Canonical Allele Identifier: CA466782135

Gene: WHRN

Linked Data

• MyVariant Identifiers: chr9:g.117170257G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114407977G>C , CM000671.2:g.114407977G>C	GRCh38
NC_000009.11:g.117170257G>C , CM000671.1:g.117170257G>C	GRCh37
NC_000009.10:g.116210078G>C	NCBI36
NG_016700.1:g.102480C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000362057.4:c.1668C>G MANE Select	ENSP00000354623.3:p.Gly556=
ENST00000673811.1:n.2392C>G
ENST00000674036.8:c.641C>G
ENST00000674048.1:n.1549C>G
ENST00000265134.10:c.519C>G	ENSP00000265134.6:p.Gly173=
ENST00000362057.3:c.1668C>G	ENSP00000354623.3:p.Gly556=
ENST00000374059.7:c.615C>G	ENSP00000363172.3:p.Gly205=
NM_001083885.2:c.519C>G	NP_001077354.2:p.Gly173=
NM_001173425.1:c.1668C>G	NP_001166896.1:p.Gly556=
NM_015404.3:c.1668C>G	NP_056219.3:p.Gly556=
XM_005251897.3:c.1005C>G	XP_005251954.2:p.Gly335=
XM_011518484.1:c.1701C>G	XP_011516786.1:p.Gly567=
XM_011518485.1:c.1701C>G	XP_011516787.1:p.Gly567=
XM_011518486.1:c.1701C>G	XP_011516788.1:p.Gly567=
XM_011518487.1:c.1575C>G	XP_011516789.1:p.Gly525=
XM_011518488.1:c.1458C>G	XP_011516790.1:p.Gly486=
XM_011518492.1:c.*53C>G	XP_011516794.1:n.*53C>G
XM_011518495.1:c.378C>G	XP_011516797.1:p.Gly126=
XR_929747.1:n.2605C>G
XR_929748.1:n.2503C>G
XR_929750.1:n.2604C>G
XR_929751.1:n.2511C>G
XR_929757.1:n.2478C>G
NM_001346890.1:c.615C>G	NP_001333819.1:p.Gly205=
XM_011518486.2:c.1701C>G	XP_011516788.1:p.Gly567=
XM_011518487.2:c.1575C>G	XP_011516789.1:p.Gly525=
XM_011518488.2:c.1458C>G	XP_011516790.1:p.Gly486=
XM_011518492.2:c.*53C>G	XP_011516794.1:n.*53C>G
XR_929747.2:n.1916C>G
XR_929748.2:n.1814C>G
XR_929750.3:n.1915C>G
XR_929757.2:n.1789C>G
NM_015404.4:c.1668C>G MANE Select	NP_056219.3:p.Gly556=
NM_001173425.2:c.1668C>G	NP_001166896.1:p.Gly556=
NM_001083885.3:c.519C>G	NP_001077354.2:p.Gly173=