Canonical Allele Identifier: CA2036979039

Gene: AMHR2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53430106_53430107delinsCT , CM000674.2:g.53430106_53430107delinsCT	GRCh38
NC_000012.11:g.53823890_53823891delinsCT , CM000674.1:g.53823890_53823891delinsCT	GRCh37
NC_000012.10:g.52110157_52110158delinsCT	NCBI36
NG_015981.1:g.11252_11253delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257863.9:c.1289-40_1289-39delinsCT MANE Select	ENSP00000257863.3:n.1289-40_1289-39delinsCT
ENST00000257863.8:c.1289-40_1289-39delinsCT	ENSP00000257863.3:n.1289-40_1289-39delinsCT
ENST00000379791.7:c.1140+481_1140+482delinsCT	ENSP00000369117.3:n.1140+481_1140+482delinsCT
ENST00000550311.5:c.1289-44_1289-43delinsCT	ENSP00000446661.1:n.1289-44_1289-43delinsCT
ENST00000550839.1:c.380-40_380-39delinsCT	ENSP00000455338.1:n.380-40_380-39delinsCT
ENST00000552233.5:n.1004_1005delinsCT
NM_001164690.1:c.1289-44_1289-43delinsCT	NP_001158162.1:n.1289-44_1289-43delinsCT
NM_001164691.1:c.1140+481_1140+482delinsCT	NP_001158163.1:n.1140+481_1140+482delinsCT
NM_020547.2:c.1289-40_1289-39delinsCT	NP_065434.1:n.1289-40_1289-39delinsCT
XM_011538173.1:c.1349-40_1349-39delinsCT	XP_011536475.1:n.1349-40_1349-39delinsCT
XM_011538174.1:c.1346-40_1346-39delinsCT	XP_011536476.1:n.1346-40_1346-39delinsCT
XM_011538175.1:c.1331-40_1331-39delinsCT	XP_011536477.1:n.1331-40_1331-39delinsCT
XM_011538176.1:c.1292-40_1292-39delinsCT	XP_011536478.1:n.1292-40_1292-39delinsCT
XM_011538177.1:c.1271-40_1271-39delinsCT	XP_011536479.1:n.1271-40_1271-39delinsCT
XM_011538178.1:c.1130-40_1130-39delinsCT	XP_011536480.1:n.1130-40_1130-39delinsCT
XM_011538179.1:c.1200+481_1200+482delinsCT	XP_011536481.1:n.1200+481_1200+482delinsCT
XM_011538180.1:c.1016-40_1016-39delinsCT	XP_011536482.1:n.1016-40_1016-39delinsCT
XM_011538181.1:c.1013-40_1013-39delinsCT	XP_011536483.1:n.1013-40_1013-39delinsCT
XM_011538182.1:c.938-40_938-39delinsCT	XP_011536484.1:n.938-40_938-39delinsCT
XM_011538183.1:c.1201-40_1201-39delinsCT	XP_011536485.1:n.1201-40_1201-39delinsCT
XM_011538184.1:c.1220+461_1220+462delinsCT	XP_011536486.1:n.1220+461_1220+462delinsCT
XM_011538185.1:c.856-1071_856-1070delinsCT	XP_011536487.1:n.856-1071_856-1070delinsCT
XM_011538186.1:c.464-40_464-39delinsCT	XP_011536488.1:n.464-40_464-39delinsCT
NM_001164690.2:c.1289-44_1289-43delinsCT	NP_001158162.1:n.1289-44_1289-43delinsCT
NM_001164691.2:c.1140+481_1140+482delinsCT	NP_001158163.1:n.1140+481_1140+482delinsCT
NM_020547.3:c.1289-40_1289-39delinsCT MANE Select	NP_065434.1:n.1289-40_1289-39delinsCT
XM_011538183.2:c.1201-40_1201-39delinsCT	XP_011536485.1:n.1201-40_1201-39delinsCT
XM_011538184.2:c.1220+461_1220+462delinsCT	XP_011536486.1:n.1220+461_1220+462delinsCT
XM_011538186.3:c.464-40_464-39delinsCT	XP_011536488.1:n.464-40_464-39delinsCT
XM_017019179.2:c.1348+128_1348+129delinsCT	XP_016874668.1:n.1348+128_1348+129delinsCT
XM_024448938.1:c.1143+481_1143+482delinsCT	XP_024304706.1:n.1143+481_1143+482delinsCT
XR_002957309.1:n.1257-40_1257-39delinsCT
XR_002957310.1:n.1109-40_1109-39delinsCT
XR_002957311.1:n.1256+128_1256+129delinsCT
XR_002957312.1:n.1108+481_1108+482delinsCT