Canonical Allele Identifier: CA2036978684

Gene: AMHR2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53429750_53429751delinsTG , CM000674.2:g.53429750_53429751delinsTG	GRCh38
NC_000012.11:g.53823534_53823535delinsTG , CM000674.1:g.53823534_53823535delinsTG	GRCh37
NC_000012.10:g.52109801_52109802delinsTG	NCBI36
NG_015981.1:g.10896_10897delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257863.9:c.1141-81_1141-80delinsTG MANE Select	ENSP00000257863.3:n.1141-81_1141-80delinsTG
ENST00000257863.8:c.1141-81_1141-80delinsTG	ENSP00000257863.3:n.1141-81_1141-80delinsTG
ENST00000379791.7:c.1140+125_1140+126delinsTG	ENSP00000369117.3:n.1140+125_1140+126delinsTG
ENST00000550311.5:c.1141-81_1141-80delinsTG	ENSP00000446661.1:n.1141-81_1141-80delinsTG
ENST00000550839.1:c.232-81_232-80delinsTG	ENSP00000455338.1:n.232-81_232-80delinsTG
ENST00000552233.5:n.648_649delinsTG
NM_001164690.1:c.1141-81_1141-80delinsTG	NP_001158162.1:n.1141-81_1141-80delinsTG
NM_001164691.1:c.1140+125_1140+126delinsTG	NP_001158163.1:n.1140+125_1140+126delinsTG
NM_020547.2:c.1141-81_1141-80delinsTG	NP_065434.1:n.1141-81_1141-80delinsTG
XM_011538173.1:c.1201-81_1201-80delinsTG	XP_011536475.1:n.1201-81_1201-80delinsTG
XM_011538174.1:c.1198-81_1198-80delinsTG	XP_011536476.1:n.1198-81_1198-80delinsTG
XM_011538175.1:c.1183-81_1183-80delinsTG	XP_011536477.1:n.1183-81_1183-80delinsTG
XM_011538176.1:c.1144-81_1144-80delinsTG	XP_011536478.1:n.1144-81_1144-80delinsTG
XM_011538177.1:c.1123-81_1123-80delinsTG	XP_011536479.1:n.1123-81_1123-80delinsTG
XM_011538178.1:c.982-81_982-80delinsTG	XP_011536480.1:n.982-81_982-80delinsTG
XM_011538179.1:c.1200+125_1200+126delinsTG	XP_011536481.1:n.1200+125_1200+126delinsTG
XM_011538180.1:c.868-81_868-80delinsTG	XP_011536482.1:n.868-81_868-80delinsTG
XM_011538181.1:c.865-81_865-80delinsTG	XP_011536483.1:n.865-81_865-80delinsTG
XM_011538182.1:c.790-81_790-80delinsTG	XP_011536484.1:n.790-81_790-80delinsTG
XM_011538183.1:c.1200+125_1200+126delinsTG	XP_011536485.1:n.1200+125_1200+126delinsTG
XM_011538184.1:c.1220+105_1220+106delinsTG	XP_011536486.1:n.1220+105_1220+106delinsTG
XM_011538185.1:c.856-1427_856-1426delinsTG	XP_011536487.1:n.856-1427_856-1426delinsTG
XM_011538186.1:c.316-81_316-80delinsTG	XP_011536488.1:n.316-81_316-80delinsTG
NM_001164690.2:c.1141-81_1141-80delinsTG	NP_001158162.1:n.1141-81_1141-80delinsTG
NM_001164691.2:c.1140+125_1140+126delinsTG	NP_001158163.1:n.1140+125_1140+126delinsTG
NM_020547.3:c.1141-81_1141-80delinsTG MANE Select	NP_065434.1:n.1141-81_1141-80delinsTG
XM_011538183.2:c.1200+125_1200+126delinsTG	XP_011536485.1:n.1200+125_1200+126delinsTG
XM_011538184.2:c.1220+105_1220+106delinsTG	XP_011536486.1:n.1220+105_1220+106delinsTG
XM_011538186.3:c.316-81_316-80delinsTG	XP_011536488.1:n.316-81_316-80delinsTG
XM_017019179.2:c.1201-81_1201-80delinsTG	XP_016874668.1:n.1201-81_1201-80delinsTG
XM_024448938.1:c.1143+125_1143+126delinsTG	XP_024304706.1:n.1143+125_1143+126delinsTG
XR_002957309.1:n.1109-81_1109-80delinsTG
XR_002957310.1:n.1108+125_1108+126delinsTG
XR_002957311.1:n.1109-81_1109-80delinsTG
XR_002957312.1:n.1108+125_1108+126delinsTG