Canonical Allele Identifier: CA2213232982
Gene: SCNN1G HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23211387_23211389delinsTTC , CM000678.2:g.23211387_23211389delinsTTC GRCh38
NC_000016.9:g.23222708_23222710delinsTTC , CM000678.1:g.23222708_23222710delinsTTC GRCh37
NC_000016.8:g.23130209_23130211delinsTTC NCBI36
NG_011909.1:g.33669_33671delinsTTC

Transcript Alleles

HGVS Amino-acid change
ENST00000300061.3:c.1177-647_1177-645delinsTTC MANE Select ENSP00000300061.2:n.1177-647_1177-645deli...
ENST00000300061.2:c.1177-647_1177-645delinsTTC ENSP00000300061.2:n.1177-647_1177-645deli...
NM_001039.3:c.1177-647_1177-645delinsTTC NP_001030.2:n.1177-647_1177-645delinsTTC
NM_001039.4:c.1177-647_1177-645delinsTTC MANE Select NP_001030.2:n.1177-647_1177-645delinsTTC