Canonical Allele Identifier: CA466911648

Gene: WHRN

Linked Data

• MyVariant Identifiers: chr9:g.117168792A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114406512A>G , CM000671.2:g.114406512A>G	GRCh38
NC_000009.11:g.117168792A>G , CM000671.1:g.117168792A>G	GRCh37
NC_000009.10:g.116208613A>G	NCBI36
NG_016700.1:g.103945T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000699485.1:c.423T>C	ENSP00000514396.1:p.Ser141=
ENST00000362057.4:c.2079T>C MANE Select	ENSP00000354623.3:p.Ser693=
ENST00000674036.8:c.1052T>C
ENST00000674048.1:n.1960T>C
ENST00000265134.10:c.930T>C	ENSP00000265134.6:p.Ser310=
ENST00000362057.3:c.2079T>C	ENSP00000354623.3:p.Ser693=
ENST00000374059.7:c.1026T>C	ENSP00000363172.3:p.Ser342=
NM_001083885.2:c.930T>C	NP_001077354.2:p.Ser310=
NM_001173425.1:c.2079T>C	NP_001166896.1:p.Ser693=
NM_015404.3:c.2079T>C	NP_056219.3:p.Ser693=
XM_005251897.3:c.1416T>C	XP_005251954.2:p.Ser472=
XM_011518484.1:c.2112T>C	XP_011516786.1:p.Ser704=
XM_011518485.1:c.2112T>C	XP_011516787.1:p.Ser704=
XM_011518486.1:c.2112T>C	XP_011516788.1:p.Ser704=
XM_011518487.1:c.1986T>C	XP_011516789.1:p.Ser662=
XM_011518488.1:c.1869T>C	XP_011516790.1:p.Ser623=
XM_011518495.1:c.789T>C	XP_011516797.1:p.Ser263=
XR_929747.1:n.3016T>C
XR_929748.1:n.2914T>C
NM_001346890.1:c.1026T>C	NP_001333819.1:p.Ser342=
XM_011518486.2:c.2112T>C	XP_011516788.1:p.Ser704=
XM_011518487.2:c.1986T>C	XP_011516789.1:p.Ser662=
XM_011518488.2:c.1869T>C	XP_011516790.1:p.Ser623=
XR_929747.2:n.2327T>C
XR_929748.2:n.2225T>C
NM_015404.4:c.2079T>C MANE Select	NP_056219.3:p.Ser693=
NM_001173425.2:c.2079T>C	NP_001166896.1:p.Ser693=
NM_001083885.3:c.930T>C	NP_001077354.2:p.Ser310=