Canonical Allele Identifier: CA1873825918

Gene: WHRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114404052C= , CM000671.2:g.114404052C=	GRCh38
NC_000009.11:g.117166332C= , CM000671.1:g.117166332C=	GRCh37
NC_000009.10:g.116206153C=	NCBI36
NG_016700.1:g.106405G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699485.1:c.606G=	ENSP00000514396.1:p.Ser202=
ENST00000362057.4:c.2262G= MANE Select	ENSP00000354623.3:p.Ser754=
ENST00000674036.8:c.1235G=
ENST00000674048.1:n.2143G=
ENST00000265134.10:c.1113G=	ENSP00000265134.6:p.Ser371=
ENST00000362057.3:c.2262G=	ENSP00000354623.3:p.Ser754=
ENST00000374059.7:c.1209G=	ENSP00000363172.3:p.Ser403=
NM_001083885.2:c.1113G=	NP_001077354.2:p.Ser371=
NM_001173425.1:c.2259G=	NP_001166896.1:p.Ser753=
NM_015404.3:c.2262G=	NP_056219.3:p.Ser754=
XM_005251897.3:c.1599G=	XP_005251954.2:p.Ser533=
XM_011518484.1:c.2295G=	XP_011516786.1:p.Ser765=
XM_011518485.1:c.2295G=	XP_011516787.1:p.Ser765=
XM_011518486.1:c.2292G=	XP_011516788.1:p.Ser764=
XM_011518487.1:c.2169G=	XP_011516789.1:p.Ser723=
XM_011518488.1:c.2052G=	XP_011516790.1:p.Ser684=
XM_011518495.1:c.972G=	XP_011516797.1:p.Ser324=
XR_929747.1:n.3199G=
XR_929748.1:n.3097G=
NM_001346890.1:c.1209G=	NP_001333819.1:p.Ser403=
XM_011518486.2:c.2292G=	XP_011516788.1:p.Ser764=
XM_011518487.2:c.2169G=	XP_011516789.1:p.Ser723=
XM_011518488.2:c.2052G=	XP_011516790.1:p.Ser684=
XR_929747.2:n.2510G=
XR_929748.2:n.2408G=
NM_015404.4:c.2262G= MANE Select	NP_056219.3:p.Ser754=
NM_001173425.2:c.2259G=	NP_001166896.1:p.Ser753=
NM_001083885.3:c.1113G=	NP_001077354.2:p.Ser371=