Canonical Allele Identifier: CA1153829845

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11845738A= , CM000663.2:g.11845738A= GRCh38
NC_000001.10:g.11905795A= , CM000663.1:g.11905795A= GRCh37
NC_000001.9:g.11828382A= NCBI36
NG_012926.1:g.7046T= , LRG_751:g.7046T=

Transcript Alleles

HGVS Amino-acid change
ENST00000400892.3:c.*1933A= (CLCN6) ENSP00000496938.1:n.*1933A=
ENST00000446542.5:n.753A= (NPPA-AS1)
ENST00000376480.7:c.*271T= (NPPA) MANE Select ENSP00000365663.3:n.*271T=
ENST00000610706.1:c.*265T= (NPPA) ENSP00000483195.1:n.*265T=
NM_006172.3:c.*271T= , LRG_751t1:c.*271T= (NPPA) NP_006163.1:n.*271T=
NR_037806.1:n.1451A= (NPPA-AS1)
NM_006172.4:c.*271T= (NPPA) MANE Select NP_006163.1:n.*271T=