Canonical Allele Identifier: CA374619024

Gene: WHRN

Linked Data

• MyVariant Identifiers: chr9:g.117165181C>G (hg19) ; chr9:g.114402901C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114402901C>G , CM000671.2:g.114402901C>G	GRCh38
NC_000009.11:g.117165181C>G , CM000671.1:g.117165181C>G	GRCh37
NC_000009.10:g.116205002C>G	NCBI36
NG_016700.1:g.107556G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699485.1:c.921G>C	ENSP00000514396.1:p.Lys307Asn
ENST00000362057.4:c.2577G>C MANE Select	ENSP00000354623.3:p.Lys859Asn
ENST00000674036.8:c.1550G>C
ENST00000674048.1:n.2458G>C
ENST00000265134.10:c.1428G>C	ENSP00000265134.6:p.Lys476Asn
ENST00000362057.3:c.2577G>C	ENSP00000354623.3:p.Lys859Asn
ENST00000374059.7:c.1524G>C	ENSP00000363172.3:p.Lys508Asn
NM_001083885.2:c.1428G>C	NP_001077354.2:p.Lys476Asn
NM_001173425.1:c.2574G>C	NP_001166896.1:p.Lys858Asn
NM_015404.3:c.2577G>C	NP_056219.3:p.Lys859Asn
XM_005251897.3:c.1914G>C	XP_005251954.2:p.Lys638Asn
XM_011518484.1:c.2610G>C	XP_011516786.1:p.Lys870Asn
XM_011518485.1:c.2610G>C	XP_011516787.1:p.Lys870Asn
XM_011518486.1:c.2607G>C	XP_011516788.1:p.Lys869Asn
XM_011518487.1:c.2484G>C	XP_011516789.1:p.Lys828Asn
XM_011518488.1:c.2367G>C	XP_011516790.1:p.Lys789Asn
XM_011518495.1:c.1287G>C	XP_011516797.1:p.Lys429Asn
NM_001346890.1:c.1524G>C	NP_001333819.1:p.Lys508Asn
XM_011518486.2:c.2607G>C	XP_011516788.1:p.Lys869Asn
XM_011518487.2:c.2484G>C	XP_011516789.1:p.Lys828Asn
XM_011518488.2:c.2367G>C	XP_011516790.1:p.Lys789Asn
NM_015404.4:c.2577G>C MANE Select	NP_056219.3:p.Lys859Asn
NM_001173425.2:c.2574G>C	NP_001166896.1:p.Lys858Asn
NM_001083885.3:c.1428G>C	NP_001077354.2:p.Lys476Asn