Canonical Allele Identifier: CA2554839688
Gene: CHRM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.137008782_137008783insG , CM000669.2:g.137008782_137008783insG GRCh38
NC_000007.13:g.136693529_136693530insG , CM000669.1:g.136693529_136693530insG GRCh37
NC_000007.12:g.136344069_136344070insG NCBI36
NG_011846.2:g.145131_145132insG , LRG_405:g.145131_145132insG

Transcript Alleles

HGVS Amino-acid change
ENST00000680005.1:c.-46-6038_-46-6037insG MANE Select ENSP00000505686.1:n.-46-6038_-46-6037insG...
ENST00000320658.9:c.-46-6038_-46-6037insG ENSP00000319984.5:n.-46-6038_-46-6037insG...
ENST00000401861.1:c.-46-6038_-46-6037insG ENSP00000384401.1:n.-46-6038_-46-6037insG...
ENST00000445907.6:c.-46-6038_-46-6037insG ENSP00000399745.2:n.-46-6038_-46-6037insG...
ENST00000453373.5:c.-46-6038_-46-6037insG ENSP00000415386.1:n.-46-6038_-46-6037insG...
NM_000739.2:c.-46-6038_-46-6037insG , LRG_405t1:c.-46-6038_-46-6037insG NP_000730.1:n.-46-6038_-46-6037insG
NM_001006626.1:c.-46-6038_-46-6037insG NP_001006627.1:n.-46-6038_-46-6037insG
NM_001006627.1:c.-46-6038_-46-6037insG NP_001006628.1:n.-46-6038_-46-6037insG
NM_001006628.1:c.-46-6038_-46-6037insG NP_001006629.1:n.-46-6038_-46-6037insG
NM_001006629.1:c.-46-6038_-46-6037insG NP_001006630.1:n.-46-6038_-46-6037insG
NM_001006630.1:c.-46-6038_-46-6037insG , LRG_405t2:c.-46-6038_-46-6037insG NP_001006631.1:n.-46-6038_-46-6037insG
NM_001006631.1:c.-46-6038_-46-6037insG NP_001006632.1:n.-46-6038_-46-6037insG
NM_001006632.1:c.-46-6038_-46-6037insG NP_001006633.1:n.-46-6038_-46-6037insG
NR_046103.1:n.341+24011_341+24012insC
XM_011515769.1:c.-46-6038_-46-6037insG XP_011514071.1:n.-46-6038_-46-6037insG
XM_011515770.1:c.-46-6038_-46-6037insG XP_011514072.1:n.-46-6038_-46-6037insG
XM_011515771.1:c.-46-6038_-46-6037insG XP_011514073.1:n.-46-6038_-46-6037insG
XM_024446648.1:c.-46-6038_-46-6037insG XP_024302416.1:n.-46-6038_-46-6037insG
NM_001006626.2:c.-46-6038_-46-6037insG NP_001006627.1:n.-46-6038_-46-6037insG
NM_001006627.2:c.-46-6038_-46-6037insG NP_001006628.1:n.-46-6038_-46-6037insG
NM_001006628.2:c.-46-6038_-46-6037insG NP_001006629.1:n.-46-6038_-46-6037insG
NM_001006629.2:c.-46-6038_-46-6037insG NP_001006630.1:n.-46-6038_-46-6037insG
NM_001006631.2:c.-46-6038_-46-6037insG NP_001006632.1:n.-46-6038_-46-6037insG
NM_001006632.2:c.-46-6038_-46-6037insG NP_001006633.1:n.-46-6038_-46-6037insG
NM_000739.3:c.-46-6038_-46-6037insG NP_000730.1:n.-46-6038_-46-6037insG
NM_001006626.3:c.-46-6038_-46-6037insG NP_001006627.1:n.-46-6038_-46-6037insG
NM_001006627.3:c.-46-6038_-46-6037insG NP_001006628.1:n.-46-6038_-46-6037insG
NM_001006628.3:c.-46-6038_-46-6037insG NP_001006629.1:n.-46-6038_-46-6037insG
NM_001006629.3:c.-46-6038_-46-6037insG NP_001006630.1:n.-46-6038_-46-6037insG
NM_001006630.2:c.-46-6038_-46-6037insG MANE Select NP_001006631.1:n.-46-6038_-46-6037insG
NM_001006631.3:c.-46-6038_-46-6037insG NP_001006632.1:n.-46-6038_-46-6037insG
NM_001006632.3:c.-46-6038_-46-6037insG NP_001006633.1:n.-46-6038_-46-6037insG
NM_001378972.1:c.-46-6038_-46-6037insG NP_001365901.1:n.-46-6038_-46-6037insG
NM_001378973.1:c.-46-6038_-46-6037insG NP_001365902.1:n.-46-6038_-46-6037insG