Canonical Allele Identifier: CA374618825

Gene: WHRN

Linked Data

• MyVariant Identifiers: chr9:g.117165082G>C (hg19) ; chr9:g.114402802G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114402802G>C , CM000671.2:g.114402802G>C	GRCh38
NC_000009.11:g.117165082G>C , CM000671.1:g.117165082G>C	GRCh37
NC_000009.10:g.116204903G>C	NCBI36
NG_016700.1:g.107655C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699485.1:c.1020C>G	ENSP00000514396.1:p.Asp340Glu
ENST00000362057.4:c.2676C>G MANE Select	ENSP00000354623.3:p.Asp892Glu
ENST00000674036.8:c.1649C>G
ENST00000674048.1:n.2557C>G
ENST00000265134.10:c.1527C>G	ENSP00000265134.6:p.Asp509Glu
ENST00000362057.3:c.2676C>G	ENSP00000354623.3:p.Asp892Glu
ENST00000374059.7:c.1623C>G	ENSP00000363172.3:p.Asp541Glu
NM_001083885.2:c.1527C>G	NP_001077354.2:p.Asp509Glu
NM_001173425.1:c.2673C>G	NP_001166896.1:p.Asp891Glu
NM_015404.3:c.2676C>G	NP_056219.3:p.Asp892Glu
XM_005251897.3:c.2013C>G	XP_005251954.2:p.Asp671Glu
XM_011518484.1:c.2709C>G	XP_011516786.1:p.Asp903Glu
XM_011518485.1:c.2709C>G	XP_011516787.1:p.Asp903Glu
XM_011518486.1:c.2706C>G	XP_011516788.1:p.Asp902Glu
XM_011518487.1:c.2583C>G	XP_011516789.1:p.Asp861Glu
XM_011518488.1:c.2466C>G	XP_011516790.1:p.Asp822Glu
XM_011518495.1:c.1386C>G	XP_011516797.1:p.Asp462Glu
NM_001346890.1:c.1623C>G	NP_001333819.1:p.Asp541Glu
XM_011518486.2:c.2706C>G	XP_011516788.1:p.Asp902Glu
XM_011518487.2:c.2583C>G	XP_011516789.1:p.Asp861Glu
XM_011518488.2:c.2466C>G	XP_011516790.1:p.Asp822Glu
NM_015404.4:c.2676C>G MANE Select	NP_056219.3:p.Asp892Glu
NM_001173425.2:c.2673C>G	NP_001166896.1:p.Asp891Glu
NM_001083885.3:c.1527C>G	NP_001077354.2:p.Asp509Glu