Canonical Allele Identifier: CA1335289456
Gene: ECEL1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232484780C= , CM000664.2:g.232484780C= GRCh38
NC_000002.11:g.233349490C= , CM000664.1:g.233349490C= GRCh37
NC_000002.10:g.233057734C= NCBI36
NG_034065.1:g.8080G=

Transcript Alleles

HGVS Amino-acid change
ENST00000304546.6:c.1059+21G= MANE Select ENSP00000302051.1:n.1059+21G=
ENST00000304546.5:c.1059+21G= ENSP00000302051.1:n.1059+21G=
ENST00000409941.1:c.1059+21G= ENSP00000386333.1:n.1059+21G=
ENST00000482346.1:n.1370+21G=
NM_001290787.1:c.1059+21G= NP_001277716.1:n.1059+21G=
NM_004826.3:c.1059+21G= NP_004817.2:n.1059+21G=
NM_004826.4:c.1059+21G= MANE Select NP_004817.2:n.1059+21G=
NM_001290787.2:c.1059+21G= NP_001277716.1:n.1059+21G=
Search 100 bp 5'
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