Canonical Allele Identifier: CA2841633038

Gene: WHRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114402849dup , CM000671.2:g.114402849dup	GRCh38
NC_000009.11:g.117165129dup , CM000671.1:g.117165129dup	GRCh37
NC_000009.10:g.116204950dup	NCBI36
NG_016700.1:g.107608dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699485.1:c.973dup	ENSP00000514396.1:p.His325ProfsTer15
ENST00000362057.4:c.2629dup MANE Select	ENSP00000354623.3:p.His877ProfsTer15
ENST00000674036.8:c.1602dup
ENST00000674048.1:n.2510dup
ENST00000265134.10:c.1480dup	ENSP00000265134.6:p.His494ProfsTer15
ENST00000362057.3:c.2629dup	ENSP00000354623.3:p.His877ProfsTer15
ENST00000374059.7:c.1576dup	ENSP00000363172.3:p.His526ProfsTer15
NM_001083885.2:c.1480dup	NP_001077354.2:p.His494ProfsTer15
NM_001173425.1:c.2626dup	NP_001166896.1:p.His876ProfsTer15
NM_015404.3:c.2629dup	NP_056219.3:p.His877ProfsTer15
XM_005251897.3:c.1966dup	XP_005251954.2:p.His656ProfsTer15
XM_011518484.1:c.2662dup	XP_011516786.1:p.His888ProfsTer15
XM_011518485.1:c.2662dup	XP_011516787.1:p.His888ProfsTer15
XM_011518486.1:c.2659dup	XP_011516788.1:p.His887ProfsTer15
XM_011518487.1:c.2536dup	XP_011516789.1:p.His846ProfsTer15
XM_011518488.1:c.2419dup	XP_011516790.1:p.His807ProfsTer15
XM_011518495.1:c.1339dup	XP_011516797.1:p.His447ProfsTer15
NM_001346890.1:c.1576dup	NP_001333819.1:p.His526ProfsTer15
XM_011518486.2:c.2659dup	XP_011516788.1:p.His887ProfsTer15
XM_011518487.2:c.2536dup	XP_011516789.1:p.His846ProfsTer15
XM_011518488.2:c.2419dup	XP_011516790.1:p.His807ProfsTer15
NM_015404.4:c.2629dup MANE Select	NP_056219.3:p.His877ProfsTer15
NM_001173425.2:c.2626dup	NP_001166896.1:p.His876ProfsTer15
NM_001083885.3:c.1480dup	NP_001077354.2:p.His494ProfsTer15