Canonical Allele Identifier: CA346156135
Gene: EMILIN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27085211C>T , CM000664.2:g.27085211C>T GRCh38
NC_000002.11:g.27308079C>T , CM000664.1:g.27308079C>T GRCh37
NC_000002.10:g.27161583C>T NCBI36
NG_012199.1:g.3469C>T
NG_046849.1:g.11645C>T
NG_012199.2:g.3469C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000380320.9:c.2627C>T MANE Select ENSP00000369677.4:p.Ala876Val
ENST00000380320.8:c.2627C>T ENSP00000369677.4:p.Ala876Val
ENST00000433140.1:c.619C>T
NM_007046.3:c.2627C>T NP_008977.1:p.Ala876Val
XM_006711928.2:c.2575+203C>T XP_006711991.1:n.2575+203C>T
NM_007046.4:c.2627C>T MANE Select NP_008977.1:p.Ala876Val