Canonical Allele Identifier: CA383552555

Gene: SCNN1A

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6347896T>G , CM000674.2:g.6347896T>G	GRCh38
NC_000012.11:g.6457062T>G , CM000674.1:g.6457062T>G	GRCh37
NC_000012.10:g.6327323T>G	NCBI36
NG_011945.1:g.34462A>C
NG_011945.2:g.34462A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000228916.7:c.1987A>C MANE Select	ENSP00000228916.2:p.Thr663Pro
ENST00000228916.6:c.1987A>C	ENSP00000228916.2:p.Thr663Pro
ENST00000338748.9:c.*1058A>C	ENSP00000345028.5:n.*1058A>C
ENST00000360168.7:c.2164A>C	ENSP00000353292.3:p.Thr722Pro
ENST00000396966.6:c.*393A>C	ENSP00000380166.2:n.*393A>C
ENST00000540037.5:c.1087A>C	ENSP00000440876.1:p.Thr363Pro
ENST00000543768.1:c.2056A>C	ENSP00000438739.1:p.Thr686Pro
NM_001038.5:c.1987A>C	NP_001029.1:p.Thr663Pro
NM_001159575.1:c.2056A>C	NP_001153047.1:p.Thr686Pro
NM_001159576.1:c.2164A>C	NP_001153048.1:p.Thr722Pro
NM_001038.6:c.1987A>C MANE Select	NP_001029.1:p.Thr663Pro
NM_001159576.2:c.2164A>C	NP_001153048.1:p.Thr722Pro
NM_001159575.2:c.2056A>C	NP_001153047.1:p.Thr686Pro