Canonical Allele Identifier: CA416107305

Linked Data

MyVariant Identifiers: chr1:g.11905792T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11845735T>C , CM000663.2:g.11845735T>C GRCh38
NC_000001.10:g.11905792T>C , CM000663.1:g.11905792T>C GRCh37
NC_000001.9:g.11828379T>C NCBI36
NG_012926.1:g.7049A>G , LRG_751:g.7049A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000400892.3:c.*1930T>C (CLCN6) ENSP00000496938.1:n.*1930T>C
ENST00000446542.5:n.750T>C (NPPA-AS1)
ENST00000376480.7:c.*274A>G (NPPA) MANE Select ENSP00000365663.3:n.*274A>G
ENST00000610706.1:c.*268A>G (NPPA) ENSP00000483195.1:n.*268A>G
NM_006172.3:c.*274A>G , LRG_751t1:c.*274A>G (NPPA) NP_006163.1:n.*274A>G
NR_037806.1:n.1448T>C (NPPA-AS1)
NM_006172.4:c.*274A>G (NPPA) MANE Select NP_006163.1:n.*274A>G