Canonical Allele Identifier: CA2785657298

Gene: WHRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114424534_114424535insACA , CM000671.2:g.114424534_114424535insACA	GRCh38
NC_000009.11:g.117186814_117186815insACA , CM000671.1:g.117186814_117186815insACA	GRCh37
NC_000009.10:g.116226635_116226636insACA	NCBI36
NG_016700.1:g.85922_85923insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699486.1:c.939_940insTGT	ENSP00000514397.1:p.Tyr313_Lys314insCys
ENST00000362057.4:c.1215_1216insTGT MANE Select	ENSP00000354623.3:p.Tyr405_Lys406insCys
ENST00000673811.1:n.2149_2150insTGT
ENST00000674036.8:c.398_399insTGT
ENST00000674048.1:n.1096_1097insTGT
ENST00000265134.10:c.66_67insTGT	ENSP00000265134.6:p.Tyr22_Lys23insCys
ENST00000362057.3:c.1215_1216insTGT	ENSP00000354623.3:p.Tyr405_Lys406insCys
ENST00000374059.7:c.162_163insTGT	ENSP00000363172.3:p.Tyr54_Lys55insCys
NM_001083885.2:c.66_67insTGT	NP_001077354.2:p.Tyr22_Lys23insCys
NM_001173425.1:c.1215_1216insTGT	NP_001166896.1:p.Tyr405_Lys406insCys
NM_015404.3:c.1215_1216insTGT	NP_056219.3:p.Tyr405_Lys406insCys
XM_005251897.3:c.964-16517_964-16516insTGT	XP_005251954.2:n.964-16517_964-16516insTGT
XM_011518484.1:c.1215_1216insTGT	XP_011516786.1:p.Tyr405_Lys406insCys
XM_011518485.1:c.1215_1216insTGT	XP_011516787.1:p.Tyr405_Lys406insCys
XM_011518486.1:c.1215_1216insTGT	XP_011516788.1:p.Tyr405_Lys406insCys
XM_011518487.1:c.1089_1090insTGT	XP_011516789.1:p.Tyr363_Lys364insCys
XM_011518488.1:c.1215_1216insTGT	XP_011516790.1:p.Tyr405_Lys406insCys
XM_011518489.1:c.1215_1216insTGT	XP_011516791.1:p.Tyr405_Lys406insCys
XM_011518490.1:c.1215_1216insTGT	XP_011516792.1:p.Tyr405_Lys406insCys
XM_011518491.1:c.1215_1216insTGT	XP_011516793.1:p.Tyr405_Lys406insCys
XM_011518492.1:c.1215_1216insTGT	XP_011516794.1:p.Tyr405_Lys406insCys
XM_011518493.1:c.1215_1216insTGT	XP_011516795.1:p.Tyr405_Lys406insCys
XM_011518494.1:c.1215_1216insTGT	XP_011516796.1:p.Tyr405_Lys406insCys
XM_011518495.1:c.-109_-108insTGT	XP_011516797.1:n.-109_-108insTGT
XR_929747.1:n.1923_1924insTGT
XR_929748.1:n.1923_1924insTGT
XR_929749.1:n.1923_1924insTGT
XR_929750.1:n.1923_1924insTGT
XR_929751.1:n.1923_1924insTGT
XR_929752.1:n.1923_1924insTGT
XR_929753.1:n.1923_1924insTGT
XR_929754.1:n.1923_1924insTGT
XR_929755.1:n.1923_1924insTGT
XR_929756.1:n.1923_1924insTGT
XR_929757.1:n.1923_1924insTGT
NM_001346890.1:c.162_163insTGT	NP_001333819.1:p.Tyr54_Lys55insCys
XM_011518486.2:c.1215_1216insTGT	XP_011516788.1:p.Tyr405_Lys406insCys
XM_011518487.2:c.1089_1090insTGT	XP_011516789.1:p.Tyr363_Lys364insCys
XM_011518488.2:c.1215_1216insTGT	XP_011516790.1:p.Tyr405_Lys406insCys
XM_011518489.3:c.1215_1216insTGT	XP_011516791.1:p.Tyr405_Lys406insCys
XM_011518491.3:c.1215_1216insTGT	XP_011516793.1:p.Tyr405_Lys406insCys
XM_011518492.2:c.1215_1216insTGT	XP_011516794.1:p.Tyr405_Lys406insCys
XM_011518494.3:c.1215_1216insTGT	XP_011516796.1:p.Tyr405_Lys406insCys
XR_929747.2:n.1234_1235insTGT
XR_929748.2:n.1234_1235insTGT
XR_929749.2:n.1234_1235insTGT
XR_929750.3:n.1234_1235insTGT
XR_929752.2:n.1234_1235insTGT
XR_929753.3:n.1234_1235insTGT
XR_929754.2:n.1234_1235insTGT
XR_929755.3:n.1234_1235insTGT
XR_929756.2:n.1234_1235insTGT
XR_929757.2:n.1234_1235insTGT
NM_015404.4:c.1215_1216insTGT MANE Select	NP_056219.3:p.Tyr405_Lys406insCys
NM_001173425.2:c.1215_1216insTGT	NP_001166896.1:p.Tyr405_Lys406insCys
NM_001083885.3:c.66_67insTGT	NP_001077354.2:p.Tyr22_Lys23insCys