Canonical Allele Identifier: CA645372378
Gene: ECEL1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232481857C>T , CM000664.2:g.232481857C>T GRCh38
NC_000002.11:g.233346567C>T , CM000664.1:g.233346567C>T GRCh37
NC_000002.10:g.233054811C>T NCBI36
NG_034065.1:g.11003G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000304546.6:c.1797-8G>A MANE Select ENSP00000302051.1:n.1797-8G>A
ENST00000304546.5:c.1797-8G>A ENSP00000302051.1:n.1797-8G>A
ENST00000409941.1:c.1791-8G>A ENSP00000386333.1:n.1791-8G>A
ENST00000411860.5:c.42-8G>A ENSP00000412683.1:n.42-8G>A
ENST00000482346.1:n.2108-8G>A
NM_001290787.1:c.1791-8G>A NP_001277716.1:n.1791-8G>A
NM_004826.3:c.1797-8G>A NP_004817.2:n.1797-8G>A
NM_004826.4:c.1797-8G>A MANE Select NP_004817.2:n.1797-8G>A
NM_001290787.2:c.1791-8G>A NP_001277716.1:n.1791-8G>A