Canonical Allele Identifier: CA1153830303

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11846168G= , CM000663.2:g.11846168G= GRCh38
NC_000001.10:g.11906225G= , CM000663.1:g.11906225G= GRCh37
NC_000001.9:g.11828812G= NCBI36
NG_012926.1:g.6616C= , LRG_751:g.6616C=

Transcript Alleles

HGVS Amino-acid change
ENST00000400892.3:c.*1961+402G= (CLCN6) ENSP00000496938.1:n.*1961+402G=
ENST00000446542.5:n.781+402G= (NPPA-AS1)
ENST00000376476.1:c.301-154C= (NPPA) ENSP00000365659.1:n.301-154C=
ENST00000376480.7:c.451-154C= (NPPA) MANE Select ENSP00000365663.3:n.451-154C=
ENST00000610706.1:c.451-154C= (NPPA) ENSP00000483195.1:n.451-154C=
NM_006172.3:c.451-154C= , LRG_751t1:c.451-154C= (NPPA) NP_006163.1:n.451-154C=
NR_037806.1:n.1479+402G= (NPPA-AS1)
NM_006172.4:c.451-154C= (NPPA) MANE Select NP_006163.1:n.451-154C=