Canonical Allele Identifier: CA2036978675

Gene: AMHR2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53429744_53429745delinsTG , CM000674.2:g.53429744_53429745delinsTG	GRCh38
NC_000012.11:g.53823528_53823529delinsTG , CM000674.1:g.53823528_53823529delinsTG	GRCh37
NC_000012.10:g.52109795_52109796delinsTG	NCBI36
NG_015981.1:g.10890_10891delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257863.9:c.1141-87_1141-86delinsTG MANE Select	ENSP00000257863.3:n.1141-87_1141-86delinsTG
ENST00000257863.8:c.1141-87_1141-86delinsTG	ENSP00000257863.3:n.1141-87_1141-86delinsTG
ENST00000379791.7:c.1140+119_1140+120delinsTG	ENSP00000369117.3:n.1140+119_1140+120delinsTG
ENST00000550311.5:c.1141-87_1141-86delinsTG	ENSP00000446661.1:n.1141-87_1141-86delinsTG
ENST00000550839.1:c.232-87_232-86delinsTG	ENSP00000455338.1:n.232-87_232-86delinsTG
ENST00000552233.5:n.642_643delinsTG
NM_001164690.1:c.1141-87_1141-86delinsTG	NP_001158162.1:n.1141-87_1141-86delinsTG
NM_001164691.1:c.1140+119_1140+120delinsTG	NP_001158163.1:n.1140+119_1140+120delinsTG
NM_020547.2:c.1141-87_1141-86delinsTG	NP_065434.1:n.1141-87_1141-86delinsTG
XM_011538173.1:c.1201-87_1201-86delinsTG	XP_011536475.1:n.1201-87_1201-86delinsTG
XM_011538174.1:c.1198-87_1198-86delinsTG	XP_011536476.1:n.1198-87_1198-86delinsTG
XM_011538175.1:c.1183-87_1183-86delinsTG	XP_011536477.1:n.1183-87_1183-86delinsTG
XM_011538176.1:c.1144-87_1144-86delinsTG	XP_011536478.1:n.1144-87_1144-86delinsTG
XM_011538177.1:c.1123-87_1123-86delinsTG	XP_011536479.1:n.1123-87_1123-86delinsTG
XM_011538178.1:c.982-87_982-86delinsTG	XP_011536480.1:n.982-87_982-86delinsTG
XM_011538179.1:c.1200+119_1200+120delinsTG	XP_011536481.1:n.1200+119_1200+120delinsTG
XM_011538180.1:c.868-87_868-86delinsTG	XP_011536482.1:n.868-87_868-86delinsTG
XM_011538181.1:c.865-87_865-86delinsTG	XP_011536483.1:n.865-87_865-86delinsTG
XM_011538182.1:c.790-87_790-86delinsTG	XP_011536484.1:n.790-87_790-86delinsTG
XM_011538183.1:c.1200+119_1200+120delinsTG	XP_011536485.1:n.1200+119_1200+120delinsTG
XM_011538184.1:c.1220+99_1220+100delinsTG	XP_011536486.1:n.1220+99_1220+100delinsTG
XM_011538185.1:c.856-1433_856-1432delinsTG	XP_011536487.1:n.856-1433_856-1432delinsTG
XM_011538186.1:c.316-87_316-86delinsTG	XP_011536488.1:n.316-87_316-86delinsTG
NM_001164690.2:c.1141-87_1141-86delinsTG	NP_001158162.1:n.1141-87_1141-86delinsTG
NM_001164691.2:c.1140+119_1140+120delinsTG	NP_001158163.1:n.1140+119_1140+120delinsTG
NM_020547.3:c.1141-87_1141-86delinsTG MANE Select	NP_065434.1:n.1141-87_1141-86delinsTG
XM_011538183.2:c.1200+119_1200+120delinsTG	XP_011536485.1:n.1200+119_1200+120delinsTG
XM_011538184.2:c.1220+99_1220+100delinsTG	XP_011536486.1:n.1220+99_1220+100delinsTG
XM_011538186.3:c.316-87_316-86delinsTG	XP_011536488.1:n.316-87_316-86delinsTG
XM_017019179.2:c.1201-87_1201-86delinsTG	XP_016874668.1:n.1201-87_1201-86delinsTG
XM_024448938.1:c.1143+119_1143+120delinsTG	XP_024304706.1:n.1143+119_1143+120delinsTG
XR_002957309.1:n.1109-87_1109-86delinsTG
XR_002957310.1:n.1108+119_1108+120delinsTG
XR_002957311.1:n.1109-87_1109-86delinsTG
XR_002957312.1:n.1108+119_1108+120delinsTG