Canonical Allele Identifier: CA2036978707

Gene: AMHR2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53429786_53429788delinsATT , CM000674.2:g.53429786_53429788delinsATT	GRCh38
NC_000012.11:g.53823570_53823572delinsATT , CM000674.1:g.53823570_53823572delinsATT	GRCh37
NC_000012.10:g.52109837_52109839delinsATT	NCBI36
NG_015981.1:g.10932_10934delinsATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257863.9:c.1141-45_1141-43delinsATT MANE Select	ENSP00000257863.3:n.1141-45_1141-43delinsATT
ENST00000257863.8:c.1141-45_1141-43delinsATT	ENSP00000257863.3:n.1141-45_1141-43delinsATT
ENST00000379791.7:c.1140+161_1140+163delinsATT	ENSP00000369117.3:n.1140+161_1140+163delinsATT
ENST00000550311.5:c.1141-45_1141-43delinsATT	ENSP00000446661.1:n.1141-45_1141-43delinsATT
ENST00000550839.1:c.232-45_232-43delinsATT	ENSP00000455338.1:n.232-45_232-43delinsATT
ENST00000552233.5:n.684_686delinsATT
NM_001164690.1:c.1141-45_1141-43delinsATT	NP_001158162.1:n.1141-45_1141-43delinsATT
NM_001164691.1:c.1140+161_1140+163delinsATT	NP_001158163.1:n.1140+161_1140+163delinsATT
NM_020547.2:c.1141-45_1141-43delinsATT	NP_065434.1:n.1141-45_1141-43delinsATT
XM_011538173.1:c.1201-45_1201-43delinsATT	XP_011536475.1:n.1201-45_1201-43delinsATT
XM_011538174.1:c.1198-45_1198-43delinsATT	XP_011536476.1:n.1198-45_1198-43delinsATT
XM_011538175.1:c.1183-45_1183-43delinsATT	XP_011536477.1:n.1183-45_1183-43delinsATT
XM_011538176.1:c.1144-45_1144-43delinsATT	XP_011536478.1:n.1144-45_1144-43delinsATT
XM_011538177.1:c.1123-45_1123-43delinsATT	XP_011536479.1:n.1123-45_1123-43delinsATT
XM_011538178.1:c.982-45_982-43delinsATT	XP_011536480.1:n.982-45_982-43delinsATT
XM_011538179.1:c.1200+161_1200+163delinsATT	XP_011536481.1:n.1200+161_1200+163delinsATT
XM_011538180.1:c.868-45_868-43delinsATT	XP_011536482.1:n.868-45_868-43delinsATT
XM_011538181.1:c.865-45_865-43delinsATT	XP_011536483.1:n.865-45_865-43delinsATT
XM_011538182.1:c.790-45_790-43delinsATT	XP_011536484.1:n.790-45_790-43delinsATT
XM_011538183.1:c.1200+161_1200+163delinsATT	XP_011536485.1:n.1200+161_1200+163delinsATT
XM_011538184.1:c.1220+141_1220+143delinsATT	XP_011536486.1:n.1220+141_1220+143delinsATT
XM_011538185.1:c.856-1391_856-1389delinsATT	XP_011536487.1:n.856-1391_856-1389delinsATT
XM_011538186.1:c.316-45_316-43delinsATT	XP_011536488.1:n.316-45_316-43delinsATT
NM_001164690.2:c.1141-45_1141-43delinsATT	NP_001158162.1:n.1141-45_1141-43delinsATT
NM_001164691.2:c.1140+161_1140+163delinsATT	NP_001158163.1:n.1140+161_1140+163delinsATT
NM_020547.3:c.1141-45_1141-43delinsATT MANE Select	NP_065434.1:n.1141-45_1141-43delinsATT
XM_011538183.2:c.1200+161_1200+163delinsATT	XP_011536485.1:n.1200+161_1200+163delinsATT
XM_011538184.2:c.1220+141_1220+143delinsATT	XP_011536486.1:n.1220+141_1220+143delinsATT
XM_011538186.3:c.316-45_316-43delinsATT	XP_011536488.1:n.316-45_316-43delinsATT
XM_017019179.2:c.1201-45_1201-43delinsATT	XP_016874668.1:n.1201-45_1201-43delinsATT
XM_024448938.1:c.1143+161_1143+163delinsATT	XP_024304706.1:n.1143+161_1143+163delinsATT
XR_002957309.1:n.1109-45_1109-43delinsATT
XR_002957310.1:n.1108+161_1108+163delinsATT
XR_002957311.1:n.1109-45_1109-43delinsATT
XR_002957312.1:n.1108+161_1108+163delinsATT