Canonical Allele Identifier: CA2451308091
Gene: AMMECR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.110264608G= , CM000685.2:g.110264608G= GRCh38
NC_000023.10:g.109507836G= , CM000685.1:g.109507836G= GRCh37
NC_000023.9:g.109394492G= NCBI36
NG_016469.1:g.180626C=
NG_016469.2:g.180626C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000686065.1:c.474-9C= ENSP00000509935.1:n.474-9C=
ENST00000262844.10:c.474-9C= MANE Select ENSP00000262844.5:n.474-9C=
ENST00000680410.1:n.441-9C=
ENST00000262844.9:c.474-9C= ENSP00000262844.5:n.474-9C=
ENST00000372057.1:c.105-9C= ENSP00000361127.1:n.105-9C=
ENST00000372059.6:c.474-47976C= ENSP00000361129.2:n.474-47976C=
ENST00000473662.1:n.174-9C=
NM_001025580.1:c.474-47976C= NP_001020751.1:n.474-47976C=
NM_001171689.1:c.105-9C= NP_001165160.1:n.105-9C=
NM_015365.2:c.474-9C= NP_056180.1:n.474-9C=
NM_015365.3:c.474-9C= MANE Select NP_056180.1:n.474-9C=
NM_001025580.2:c.474-47976C= NP_001020751.1:n.474-47976C=
NM_001171689.2:c.105-9C= NP_001165160.1:n.105-9C=