Canonical Allele Identifier: CA2213223904
Gene: SCNN1G HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23196817_23196820delinsGGGA , CM000678.2:g.23196817_23196820delinsGGGA GRCh38
NC_000016.9:g.23208138_23208141delinsGGGA , CM000678.1:g.23208138_23208141delinsGGGA GRCh37
NC_000016.8:g.23115639_23115642delinsGGGA NCBI36
NG_011909.1:g.19099_19102delinsGGGA

Transcript Alleles

HGVS Amino-acid change
ENST00000300061.3:c.914-447_914-444delinsGGGA MANE Select ENSP00000300061.2:n.914-447_914-444delins...
ENST00000300061.2:c.914-447_914-444delinsGGGA ENSP00000300061.2:n.914-447_914-444delins...
NM_001039.3:c.914-447_914-444delinsGGGA NP_001030.2:n.914-447_914-444delinsGGGA
NM_001039.4:c.914-447_914-444delinsGGGA MANE Select NP_001030.2:n.914-447_914-444delinsGGGA