Canonical Allele Identifier: CA374620348

Gene: WHRN

Linked Data

• MyVariant Identifiers: chr9:g.117168794A>T (hg19) ; chr9:g.114406514A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114406514A>T , CM000671.2:g.114406514A>T	GRCh38
NC_000009.11:g.117168794A>T , CM000671.1:g.117168794A>T	GRCh37
NC_000009.10:g.116208615A>T	NCBI36
NG_016700.1:g.103943T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000699485.1:c.421T>A	ENSP00000514396.1:p.Ser141Thr
ENST00000362057.4:c.2077T>A MANE Select	ENSP00000354623.3:p.Ser693Thr
ENST00000674036.8:c.1050T>A
ENST00000674048.1:n.1958T>A
ENST00000265134.10:c.928T>A	ENSP00000265134.6:p.Ser310Thr
ENST00000362057.3:c.2077T>A	ENSP00000354623.3:p.Ser693Thr
ENST00000374059.7:c.1024T>A	ENSP00000363172.3:p.Ser342Thr
NM_001083885.2:c.928T>A	NP_001077354.2:p.Ser310Thr
NM_001173425.1:c.2077T>A	NP_001166896.1:p.Ser693Thr
NM_015404.3:c.2077T>A	NP_056219.3:p.Ser693Thr
XM_005251897.3:c.1414T>A	XP_005251954.2:p.Ser472Thr
XM_011518484.1:c.2110T>A	XP_011516786.1:p.Ser704Thr
XM_011518485.1:c.2110T>A	XP_011516787.1:p.Ser704Thr
XM_011518486.1:c.2110T>A	XP_011516788.1:p.Ser704Thr
XM_011518487.1:c.1984T>A	XP_011516789.1:p.Ser662Thr
XM_011518488.1:c.1867T>A	XP_011516790.1:p.Ser623Thr
XM_011518495.1:c.787T>A	XP_011516797.1:p.Ser263Thr
XR_929747.1:n.3014T>A
XR_929748.1:n.2912T>A
NM_001346890.1:c.1024T>A	NP_001333819.1:p.Ser342Thr
XM_011518486.2:c.2110T>A	XP_011516788.1:p.Ser704Thr
XM_011518487.2:c.1984T>A	XP_011516789.1:p.Ser662Thr
XM_011518488.2:c.1867T>A	XP_011516790.1:p.Ser623Thr
XR_929747.2:n.2325T>A
XR_929748.2:n.2223T>A
NM_015404.4:c.2077T>A MANE Select	NP_056219.3:p.Ser693Thr
NM_001173425.2:c.2077T>A	NP_001166896.1:p.Ser693Thr
NM_001083885.3:c.928T>A	NP_001077354.2:p.Ser310Thr