Canonical Allele Identifier: CA1597039020

Gene: HMMR HMMR-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.163490702G= , CM000667.2:g.163490702G=	GRCh38
NC_000005.9:g.162917708G= , CM000667.1:g.162917708G=	GRCh37
NC_000005.8:g.162850286G=	NCBI36
NG_023309.1:g.35192G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393915.9:c.2125+150G= (HMMR) MANE Select	ENSP00000377492.4:n.2125+150G=
ENST00000353866.7:c.2077+150G= (HMMR)	ENSP00000185942.6:n.2077+150G=
ENST00000358715.3:c.2122+150G= (HMMR)	ENSP00000351554.3:n.2122+150G=
ENST00000393915.8:c.2125+150G= (HMMR)	ENSP00000377492.4:n.2125+150G=
ENST00000432118.6:c.1864+150G= (HMMR)	ENSP00000402673.2:n.1864+150G=
NM_001142556.1:c.2125+150G= (HMMR)	NP_001136028.1:n.2125+150G=
NM_001142557.1:c.1864+150G= (HMMR)	NP_001136029.1:n.1864+150G=
NM_012484.2:c.2122+150G= (HMMR)	NP_036616.2:n.2122+150G=
NM_012485.2:c.2077+150G= (HMMR)	NP_036617.2:n.2077+150G=
NR_109892.1:n.468-1319C= (HMMR-AS1)
NM_001142556.2:c.2125+150G= (HMMR) MANE Select	NP_001136028.1:n.2125+150G=
NM_001142557.2:c.1864+150G= (HMMR)	NP_001136029.1:n.1864+150G=
NM_012484.3:c.2122+150G= (HMMR)	NP_036616.2:n.2122+150G=
NM_012485.3:c.2077+150G= (HMMR)	NP_036617.2:n.2077+150G=