Canonical Allele Identifier: CA374618904

Gene: WHRN

Linked Data

• gnomAD v4: 9-114402840-C-A
• MyVariant Identifiers: chr9:g.117165120C>A (hg19) ; chr9:g.114402840C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114402840C>A , CM000671.2:g.114402840C>A	GRCh38
NC_000009.11:g.117165120C>A , CM000671.1:g.117165120C>A	GRCh37
NC_000009.10:g.116204941C>A	NCBI36
NG_016700.1:g.107617G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699485.1:c.982G>T	ENSP00000514396.1:p.Ala328Ser
ENST00000362057.4:c.2638G>T MANE Select	ENSP00000354623.3:p.Ala880Ser
ENST00000674036.8:c.1611G>T
ENST00000674048.1:n.2519G>T
ENST00000265134.10:c.1489G>T	ENSP00000265134.6:p.Ala497Ser
ENST00000362057.3:c.2638G>T	ENSP00000354623.3:p.Ala880Ser
ENST00000374059.7:c.1585G>T	ENSP00000363172.3:p.Ala529Ser
NM_001083885.2:c.1489G>T	NP_001077354.2:p.Ala497Ser
NM_001173425.1:c.2635G>T	NP_001166896.1:p.Ala879Ser
NM_015404.3:c.2638G>T	NP_056219.3:p.Ala880Ser
XM_005251897.3:c.1975G>T	XP_005251954.2:p.Ala659Ser
XM_011518484.1:c.2671G>T	XP_011516786.1:p.Ala891Ser
XM_011518485.1:c.2671G>T	XP_011516787.1:p.Ala891Ser
XM_011518486.1:c.2668G>T	XP_011516788.1:p.Ala890Ser
XM_011518487.1:c.2545G>T	XP_011516789.1:p.Ala849Ser
XM_011518488.1:c.2428G>T	XP_011516790.1:p.Ala810Ser
XM_011518495.1:c.1348G>T	XP_011516797.1:p.Ala450Ser
NM_001346890.1:c.1585G>T	NP_001333819.1:p.Ala529Ser
XM_011518486.2:c.2668G>T	XP_011516788.1:p.Ala890Ser
XM_011518487.2:c.2545G>T	XP_011516789.1:p.Ala849Ser
XM_011518488.2:c.2428G>T	XP_011516790.1:p.Ala810Ser
NM_015404.4:c.2638G>T MANE Select	NP_056219.3:p.Ala880Ser
NM_001173425.2:c.2635G>T	NP_001166896.1:p.Ala879Ser
NM_001083885.3:c.1489G>T	NP_001077354.2:p.Ala497Ser