Canonical Allele Identifier: CA1240109535
Gene: EMILIN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27084919_27084922delinsTCAG , CM000664.2:g.27084919_27084922delinsTCAG GRCh38
NC_000002.11:g.27307787_27307790delinsTCAG , CM000664.1:g.27307787_27307790delinsTCAG GRCh37
NC_000002.10:g.27161291_27161294delinsTCAG NCBI36
NG_012199.1:g.3177_3180delinsTCAG
NG_046849.1:g.11353_11356delinsTCAG
NG_012199.2:g.3177_3180delinsTCAG

Transcript Alleles

HGVS Amino-acid change
ENST00000380320.9:c.2558-72_2558-69delinsTCAG MANE Select ENSP00000369677.4:n.2558-72_2558-69delins...
ENST00000380320.8:c.2558-72_2558-69delinsTCAG ENSP00000369677.4:n.2558-72_2558-69delins...
ENST00000433140.1:c.550-72_550-69delinsTCAG
NM_007046.3:c.2558-72_2558-69delinsTCAG NP_008977.1:n.2558-72_2558-69delinsTCAG
XM_006711928.2:c.2558-72_2558-69delinsTCAG XP_006711991.1:n.2558-72_2558-69delinsTCA...
NM_007046.4:c.2558-72_2558-69delinsTCAG MANE Select NP_008977.1:n.2558-72_2558-69delinsTCAG