Canonical Allele Identifier: CA346156183
Gene: EMILIN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27085225C>G , CM000664.2:g.27085225C>G GRCh38
NC_000002.11:g.27308093C>G , CM000664.1:g.27308093C>G GRCh37
NC_000002.10:g.27161597C>G NCBI36
NG_012199.1:g.3483C>G
NG_046849.1:g.11659C>G
NG_012199.2:g.3483C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000380320.9:c.2641C>G MANE Select ENSP00000369677.4:p.Arg881Gly
ENST00000380320.8:c.2641C>G ENSP00000369677.4:p.Arg881Gly
ENST00000433140.1:c.633C>G
NM_007046.3:c.2641C>G NP_008977.1:p.Arg881Gly
XM_006711928.2:c.2575+217C>G XP_006711991.1:n.2575+217C>G
NM_007046.4:c.2641C>G MANE Select NP_008977.1:p.Arg881Gly