Canonical Allele Identifier: CA1335289432
Gene: ECEL1 HGNC NCBI

Linked Data

dbSNP Id: rs1575077681

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232484766A>C , CM000664.2:g.232484766A>C GRCh38
NC_000002.11:g.233349476A>C , CM000664.1:g.233349476A>C GRCh37
NC_000002.10:g.233057720A>C NCBI36
NG_034065.1:g.8094T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000304546.6:c.1059+35T>G MANE Select ENSP00000302051.1:n.1059+35T>G
ENST00000304546.5:c.1059+35T>G ENSP00000302051.1:n.1059+35T>G
ENST00000409941.1:c.1059+35T>G ENSP00000386333.1:n.1059+35T>G
ENST00000482346.1:n.1370+35T>G
NM_001290787.1:c.1059+35T>G NP_001277716.1:n.1059+35T>G
NM_004826.3:c.1059+35T>G NP_004817.2:n.1059+35T>G
NM_004826.4:c.1059+35T>G MANE Select NP_004817.2:n.1059+35T>G
NM_001290787.2:c.1059+35T>G NP_001277716.1:n.1059+35T>G