Canonical Allele Identifier: CA1597027545
Gene: HMMR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.163478574G= , CM000667.2:g.163478574G= GRCh38
NC_000005.9:g.162905580G= , CM000667.1:g.162905580G= GRCh37
NC_000005.8:g.162838158G= NCBI36
NG_023309.1:g.23064G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000393915.9:c.1269-110G= MANE Select ENSP00000377492.4:n.1269-110G=
ENST00000353866.7:c.1221-110G= ENSP00000185942.6:n.1221-110G=
ENST00000358715.3:c.1266-110G= ENSP00000351554.3:n.1266-110G=
ENST00000393915.8:c.1269-110G= ENSP00000377492.4:n.1269-110G=
ENST00000432118.6:c.1008-110G= ENSP00000402673.2:n.1008-110G=
NM_001142556.1:c.1269-110G= NP_001136028.1:n.1269-110G=
NM_001142557.1:c.1008-110G= NP_001136029.1:n.1008-110G=
NM_012484.2:c.1266-110G= NP_036616.2:n.1266-110G=
NM_012485.2:c.1221-110G= NP_036617.2:n.1221-110G=
NM_001142556.2:c.1269-110G= MANE Select NP_001136028.1:n.1269-110G=
NM_001142557.2:c.1008-110G= NP_001136029.1:n.1008-110G=
NM_012484.3:c.1266-110G= NP_036616.2:n.1266-110G=
NM_012485.3:c.1221-110G= NP_036617.2:n.1221-110G=