Canonical Allele Identifier: CA2619053383
Gene: AMHR2 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000257863.9:c.1289-40dup MANE Select ENSP00000257863.3:n.1289-40dup
ENST00000257863.8:c.1289-40dup ENSP00000257863.3:n.1289-40dup
ENST00000379791.7:c.1140+481dup ENSP00000369117.3:n.1140+481dup
ENST00000550311.5:c.1289-44dup ENSP00000446661.1:n.1289-44dup
ENST00000550839.1:c.380-40dup ENSP00000455338.1:n.380-40dup
ENST00000552233.5:n.1004dup
NM_001164690.1:c.1289-44dup NP_001158162.1:n.1289-44dup
NM_001164691.1:c.1140+481dup NP_001158163.1:n.1140+481dup
NM_020547.2:c.1289-40dup NP_065434.1:n.1289-40dup
XM_011538173.1:c.1349-40dup XP_011536475.1:n.1349-40dup
XM_011538174.1:c.1346-40dup XP_011536476.1:n.1346-40dup
XM_011538175.1:c.1331-40dup XP_011536477.1:n.1331-40dup
XM_011538176.1:c.1292-40dup XP_011536478.1:n.1292-40dup
XM_011538177.1:c.1271-40dup XP_011536479.1:n.1271-40dup
XM_011538178.1:c.1130-40dup XP_011536480.1:n.1130-40dup
XM_011538179.1:c.1200+481dup XP_011536481.1:n.1200+481dup
XM_011538180.1:c.1016-40dup XP_011536482.1:n.1016-40dup
XM_011538181.1:c.1013-40dup XP_011536483.1:n.1013-40dup
XM_011538182.1:c.938-40dup XP_011536484.1:n.938-40dup
XM_011538183.1:c.1201-40dup XP_011536485.1:n.1201-40dup
XM_011538184.1:c.1220+461dup XP_011536486.1:n.1220+461dup
XM_011538185.1:c.856-1071dup XP_011536487.1:n.856-1071dup
XM_011538186.1:c.464-40dup XP_011536488.1:n.464-40dup
NM_001164690.2:c.1289-44dup NP_001158162.1:n.1289-44dup
NM_001164691.2:c.1140+481dup NP_001158163.1:n.1140+481dup
NM_020547.3:c.1289-40dup MANE Select NP_065434.1:n.1289-40dup
XM_011538183.2:c.1201-40dup XP_011536485.1:n.1201-40dup
XM_011538184.2:c.1220+461dup XP_011536486.1:n.1220+461dup
XM_011538186.3:c.464-40dup XP_011536488.1:n.464-40dup
XM_017019179.2:c.1348+128dup XP_016874668.1:n.1348+128dup
XM_024448938.1:c.1143+481dup XP_024304706.1:n.1143+481dup
XR_002957309.1:n.1257-40dup
XR_002957310.1:n.1109-40dup
XR_002957311.1:n.1256+128dup
XR_002957312.1:n.1108+481dup