Canonical Allele Identifier: CA2451308070
Gene: AMMECR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.110264486C= , CM000685.2:g.110264486C= GRCh38
NC_000023.10:g.109507714C= , CM000685.1:g.109507714C= GRCh37
NC_000023.9:g.109394370C= NCBI36
NG_016469.1:g.180748G=
NG_016469.2:g.180748G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000686065.1:c.584+3G= ENSP00000509935.1:n.584+3G=
ENST00000262844.10:c.584+3G= MANE Select ENSP00000262844.5:n.584+3G=
ENST00000680410.1:n.551+3G=
ENST00000262844.9:c.584+3G= ENSP00000262844.5:n.584+3G=
ENST00000372057.1:c.215+3G= ENSP00000361127.1:n.215+3G=
ENST00000372059.6:c.474-47854G= ENSP00000361129.2:n.474-47854G=
ENST00000473662.1:n.284+3G=
NM_001025580.1:c.474-47854G= NP_001020751.1:n.474-47854G=
NM_001171689.1:c.215+3G= NP_001165160.1:n.215+3G=
NM_015365.2:c.584+3G= NP_056180.1:n.584+3G=
NM_015365.3:c.584+3G= MANE Select NP_056180.1:n.584+3G=
NM_001025580.2:c.474-47854G= NP_001020751.1:n.474-47854G=
NM_001171689.2:c.215+3G= NP_001165160.1:n.215+3G=