Canonical Allele Identifier: CA2036978796

Gene: AMHR2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53429892_53429909delinsGGGGCATGGCCCTCCGAC , CM000674.2:g.53429892_53429909delinsGGGGCATGGCCCTCCGAC	GRCh38
NC_000012.11:g.53823676_53823693delinsGGGGCATGGCCCTCCGAC , CM000674.1:g.53823676_53823693delinsGGGGCATGGCCCTCCGAC	GRCh37
NC_000012.10:g.52109943_52109960delinsGGGGCATGGCCCTCCGAC	NCBI36
NG_015981.1:g.11038_11055delinsGGGGCATGGCCCTCCGAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000257863.9:c.1202_1219delinsGGGGCATGGCCCTCCGAC MANE Select	ENSP00000257863.3:p.Trp401=
ENST00000257863.8:c.1202_1219delinsGGGGCATGGCCCTCCGAC	ENSP00000257863.3:p.Trp401=
ENST00000379791.7:c.1140+267_1140+284delinsGGGGCATGGCCCTCCGAC	ENSP00000369117.3:n.1140+267_1140+284deli...
ENST00000550311.5:c.1202_1219delinsGGGGCATGGCCCTCCGAC	ENSP00000446661.1:p.Trp401=
ENST00000550839.1:c.293_310delinsGGGGCATGGCCCTCCGAC	ENSP00000455338.1:p.Trp98=
ENST00000552233.5:n.790_807delinsGGGGCATGGCCCTCCGAC
NM_001164690.1:c.1202_1219delinsGGGGCATGGCCCTCCGAC	NP_001158162.1:p.Trp401=
NM_001164691.1:c.1140+267_1140+284delinsGGGGCATGGCCCTCCGAC	NP_001158163.1:n.1140+267_1140+284delinsG...
NM_020547.2:c.1202_1219delinsGGGGCATGGCCCTCCGAC	NP_065434.1:p.Trp401=
XM_011538173.1:c.1262_1279delinsGGGGCATGGCCCTCCGAC	XP_011536475.1:p.Trp421=
XM_011538174.1:c.1259_1276delinsGGGGCATGGCCCTCCGAC	XP_011536476.1:p.Trp420=
XM_011538175.1:c.1244_1261delinsGGGGCATGGCCCTCCGAC	XP_011536477.1:p.Trp415=
XM_011538176.1:c.1205_1222delinsGGGGCATGGCCCTCCGAC	XP_011536478.1:p.Trp402=
XM_011538177.1:c.1184_1201delinsGGGGCATGGCCCTCCGAC	XP_011536479.1:p.Trp395=
XM_011538178.1:c.1043_1060delinsGGGGCATGGCCCTCCGAC	XP_011536480.1:p.Trp348=
XM_011538179.1:c.1200+267_1200+284delinsGGGGCATGGCCCTCCGAC	XP_011536481.1:n.1200+267_1200+284delinsG...
XM_011538180.1:c.929_946delinsGGGGCATGGCCCTCCGAC	XP_011536482.1:p.Trp310=
XM_011538181.1:c.926_943delinsGGGGCATGGCCCTCCGAC	XP_011536483.1:p.Trp309=
XM_011538182.1:c.851_868delinsGGGGCATGGCCCTCCGAC	XP_011536484.1:p.Trp284=
XM_011538183.1:c.1201-254_1201-237delinsGGGGCATGGCCCTCCGAC	XP_011536485.1:n.1201-254_1201-237delinsG...
XM_011538184.1:c.1220+247_1220+264delinsGGGGCATGGCCCTCCGAC	XP_011536486.1:n.1220+247_1220+264delinsG...
XM_011538185.1:c.856-1285_856-1268delinsGGGGCATGGCCCTCCGAC	XP_011536487.1:n.856-1285_856-1268delinsG...
XM_011538186.1:c.377_394delinsGGGGCATGGCCCTCCGAC	XP_011536488.1:p.Trp126=
NM_001164690.2:c.1202_1219delinsGGGGCATGGCCCTCCGAC	NP_001158162.1:p.Trp401=
NM_001164691.2:c.1140+267_1140+284delinsGGGGCATGGCCCTCCGAC	NP_001158163.1:n.1140+267_1140+284delinsG...
NM_020547.3:c.1202_1219delinsGGGGCATGGCCCTCCGAC MANE Select	NP_065434.1:p.Trp401=
XM_011538183.2:c.1201-254_1201-237delinsGGGGCATGGCCCTCCGAC	XP_011536485.1:n.1201-254_1201-237delinsG...
XM_011538184.2:c.1220+247_1220+264delinsGGGGCATGGCCCTCCGAC	XP_011536486.1:n.1220+247_1220+264delinsG...
XM_011538186.3:c.377_394delinsGGGGCATGGCCCTCCGAC	XP_011536488.1:p.Trp126=
XM_017019179.2:c.1262_1279delinsGGGGCATGGCCCTCCGAC	XP_016874668.1:p.Trp421=
XM_024448938.1:c.1143+267_1143+284delinsGGGGCATGGCCCTCCGAC	XP_024304706.1:n.1143+267_1143+284delinsG...
XR_002957309.1:n.1170_1187delinsGGGGCATGGCCCTCCGAC
XR_002957310.1:n.1109-254_1109-237delinsGGGGCATGGCCCTCCGAC
XR_002957311.1:n.1170_1187delinsGGGGCATGGCCCTCCGAC
XR_002957312.1:n.1108+267_1108+284delinsGGGGCATGGCCCTCCGAC