Canonical Allele Identifier: CA2822950387
Gene: AMMECR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.110264599_110264600insTAGGGCTCGTTGGTGAATCGGGGGGTCCGGGGCTGCTGGTATCCATACAGGTGACAGTAGAGCACATCGAAGCAAAAGCAGCA , CM000685.2:g.110264599_110264600insTAGGGCTCGTTGGTGAATCGGGGGGTCCGGGGCTGCTGGTATCCATACAGGTGACAGTAGAGCACATCGAAGCAAAAGCAGCA GRCh38
NC_000023.10:g.109507827_109507828insTAGGGCTCGTTGGTGAATCGGGGGGTCCGGGGCTGCTGGTATCCATACAGGTGACAGTAGAGCACATCGAAGCAAAAGCAGCA , CM000685.1:g.109507827_109507828insTAGGGCTCGTTGGTGAATCGGGGGGTCCGGGGCTGCTGGTATCCATACAGGTGACAGTAGAGCACATCGAAGCAAAAGCAGCA GRCh37
NC_000023.9:g.109394483_109394484insTAGGGCTCGTTGGTGAATCGGGGGGTCCGGGGCTGCTGGTATCCATACAGGTGACAGTAGAGCACATCGAAGCAAAAGCAGCA NCBI36
NG_016469.1:g.180634_180635insTGCTGCTTTTGCTTCGATGTGCTCTACTGTCACCTGTATGGATACCAGCAGCCCCGGACCCCCCGATTCACCAACGAGCCCTA
NG_016469.2:g.180634_180635insTGCTGCTTTTGCTTCGATGTGCTCTACTGTCACCTGTATGGATACCAGCAGCCCCGGACCCCCCGATTCACCAACGAGCCCTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000686065.1:c.474-1_474insTGCTGCTTTTGCTTCGATGTGCTCTACTGTCACCTGTATGGATACCAGCAGCCCCGGACCCCCCGATTCACCAACGAGCCCTA ENSP00000509935.1:n.474-1_474insTGCTGCTTTTGCTTCGATGTGCTCTACTG...
ENST00000262844.10:c.474-1_474insTGCTGCTTTTGCTTCGATGTGCTCTACTGTCACCTGTATGGATACCAGCAGCCCCGGACCCCCCGATTCACCAACGAGCCCTA MANE Select ENSP00000262844.5:n.474-1_474insTGCTGCTTTTGCTTCGATGTGCTCTACTG...
ENST00000680410.1:n.441-1_441insTGCTGCTTTTGCTTCGATGTGCTCTACTGTCACCTGTATGGATACCAGCAGCCCCGGACCCCCCGATTCACCAACGAGCCCTA
ENST00000262844.9:c.474-1_474insTGCTGCTTTTGCTTCGATGTGCTCTACTGTCACCTGTATGGATACCAGCAGCCCCGGACCCCCCGATTCACCAACGAGCCCTA ENSP00000262844.5:n.474-1_474insTGCTGCTTTTGCTTCGATGTGCTCTACTG...
ENST00000372057.1:c.105-1_105insTGCTGCTTTTGCTTCGATGTGCTCTACTGTCACCTGTATGGATACCAGCAGCCCCGGACCCCCCGATTCACCAACGAGCCCTA ENSP00000361127.1:n.105-1_105insTGCTGCTTTTGCTTCGATGTGCTCTACTG...
ENST00000372059.6:c.474-47968_474-47967insTGCTGCTTTTGCTTCGATGTGCTCTACTGTCACCTGTATGGATACCAGCAGCCCCGGACCCCCCGATTCACCAACGAGCCCTA ENSP00000361129.2:n.474-47968_474-47967insTGCTGCTTTTGCTTCGATG...
ENST00000473662.1:n.174-1_174insTGCTGCTTTTGCTTCGATGTGCTCTACTGTCACCTGTATGGATACCAGCAGCCCCGGACCCCCCGATTCACCAACGAGCCCTA
NM_001025580.1:c.474-47968_474-47967insTGCTGCTTTTGCTTCGATGTGCTCTACTGTCACCTGTATGGATACCAGCAGCCCCGGACCCCCCGATTCACCAACGAGCCCTA NP_001020751.1:n.474-47968_474-47967insTGCTGCTTTTGCTTCGATGTGC...
NM_001171689.1:c.105-1_105insTGCTGCTTTTGCTTCGATGTGCTCTACTGTCACCTGTATGGATACCAGCAGCCCCGGACCCCCCGATTCACCAACGAGCCCTA NP_001165160.1:n.105-1_105insTGCTGCTTTTGCTTCGATGTGCTCTACTGTCA...
NM_015365.2:c.474-1_474insTGCTGCTTTTGCTTCGATGTGCTCTACTGTCACCTGTATGGATACCAGCAGCCCCGGACCCCCCGATTCACCAACGAGCCCTA NP_056180.1:n.474-1_474insTGCTGCTTTTGCTTCGATGTGCTCTACTGTCACCT...
NM_015365.3:c.474-1_474insTGCTGCTTTTGCTTCGATGTGCTCTACTGTCACCTGTATGGATACCAGCAGCCCCGGACCCCCCGATTCACCAACGAGCCCTA MANE Select NP_056180.1:n.474-1_474insTGCTGCTTTTGCTTCGATGTGCTCTACTGTCACCT...
NM_001025580.2:c.474-47968_474-47967insTGCTGCTTTTGCTTCGATGTGCTCTACTGTCACCTGTATGGATACCAGCAGCCCCGGACCCCCCGATTCACCAACGAGCCCTA NP_001020751.1:n.474-47968_474-47967insTGCTGCTTTTGCTTCGATGTGC...
NM_001171689.2:c.105-1_105insTGCTGCTTTTGCTTCGATGTGCTCTACTGTCACCTGTATGGATACCAGCAGCCCCGGACCCCCCGATTCACCAACGAGCCCTA NP_001165160.1:n.105-1_105insTGCTGCTTTTGCTTCGATGTGCTCTACTGTCA...