Canonical Allele Identifier: CA858990231

Gene: WHRN

Linked Data

• dbSNP Id: rs1191732949
• MyVariant Identifiers: chr9:g.117170335_117170336insGCTGAGAAGGGAAC (hg19) ; chr9:g.114408055_114408056insGCTGAGAAGGGAAC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114408056_114408069dup , CM000671.2:g.114408056_114408069dup	GRCh38
NC_000009.11:g.117170336_117170349dup , CM000671.1:g.117170336_117170349dup	GRCh37
NC_000009.10:g.116210157_116210170dup	NCBI36
NG_016700.1:g.102388_102401dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362057.4:c.1627-51_1627-38dup MANE Select	ENSP00000354623.3:n.1627-51_1627-38dup
ENST00000673811.1:n.2351-51_2351-38dup
ENST00000674036.8:c.600-51_600-38dup
ENST00000674048.1:n.1508-51_1508-38dup
ENST00000265134.10:c.478-51_478-38dup	ENSP00000265134.6:n.478-51_478-38dup
ENST00000362057.3:c.1627-51_1627-38dup	ENSP00000354623.3:n.1627-51_1627-38dup
ENST00000374059.7:c.574-51_574-38dup	ENSP00000363172.3:n.574-51_574-38dup
NM_001083885.2:c.478-51_478-38dup	NP_001077354.2:n.478-51_478-38dup
NM_001173425.1:c.1627-51_1627-38dup	NP_001166896.1:n.1627-51_1627-38dup
NM_015404.3:c.1627-51_1627-38dup	NP_056219.3:n.1627-51_1627-38dup
XM_005251897.3:c.964-51_964-38dup	XP_005251954.2:n.964-51_964-38dup
XM_011518484.1:c.1660-51_1660-38dup	XP_011516786.1:n.1660-51_1660-38dup
XM_011518485.1:c.1660-51_1660-38dup	XP_011516787.1:n.1660-51_1660-38dup
XM_011518486.1:c.1660-51_1660-38dup	XP_011516788.1:n.1660-51_1660-38dup
XM_011518487.1:c.1534-51_1534-38dup	XP_011516789.1:n.1534-51_1534-38dup
XM_011518488.1:c.1417-51_1417-38dup	XP_011516790.1:n.1417-51_1417-38dup
XM_011518492.1:c.*12-51_*12-38dup	XP_011516794.1:n.*12-51_*12-38dup
XM_011518495.1:c.337-51_337-38dup	XP_011516797.1:n.337-51_337-38dup
XR_929747.1:n.2564-51_2564-38dup
XR_929748.1:n.2462-51_2462-38dup
XR_929750.1:n.2563-51_2563-38dup
XR_929751.1:n.2470-51_2470-38dup
XR_929757.1:n.2437-51_2437-38dup
NM_001346890.1:c.574-51_574-38dup	NP_001333819.1:n.574-51_574-38dup
XM_011518486.2:c.1660-51_1660-38dup	XP_011516788.1:n.1660-51_1660-38dup
XM_011518487.2:c.1534-51_1534-38dup	XP_011516789.1:n.1534-51_1534-38dup
XM_011518488.2:c.1417-51_1417-38dup	XP_011516790.1:n.1417-51_1417-38dup
XM_011518492.2:c.*12-51_*12-38dup	XP_011516794.1:n.*12-51_*12-38dup
XR_929747.2:n.1875-51_1875-38dup
XR_929748.2:n.1773-51_1773-38dup
XR_929750.3:n.1874-51_1874-38dup
XR_929757.2:n.1748-51_1748-38dup
NM_015404.4:c.1627-51_1627-38dup MANE Select	NP_056219.3:n.1627-51_1627-38dup
NM_001173425.2:c.1627-51_1627-38dup	NP_001166896.1:n.1627-51_1627-38dup
NM_001083885.3:c.478-51_478-38dup	NP_001077354.2:n.478-51_478-38dup