Canonical Allele Identifier: CA2658283555
Gene: EMILIN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27085166del , CM000664.2:g.27085166del GRCh38
NC_000002.11:g.27308034del , CM000664.1:g.27308034del GRCh37
NC_000002.10:g.27161538del NCBI36
NG_012199.1:g.3424del
NG_046849.1:g.11600del
NG_012199.2:g.3424del

Transcript Alleles

HGVS Amino-acid Change
ENST00000380320.9:c.2582del MANE Select ENSP00000369677.4:p.Glu861GlyfsTer17
ENST00000380320.8:c.2582del ENSP00000369677.4:p.Glu861GlyfsTer17
ENST00000433140.1:c.574del
NM_007046.3:c.2582del NP_008977.1:p.Glu861GlyfsTer17
XM_006711928.2:c.2575+158del XP_006711991.1:n.2575+158del
NM_007046.4:c.2582del MANE Select NP_008977.1:p.Glu861GlyfsTer17