Canonical Allele Identifier: CA1240109529
Gene: EMILIN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27084909C= , CM000664.2:g.27084909C= GRCh38
NC_000002.11:g.27307777C= , CM000664.1:g.27307777C= GRCh37
NC_000002.10:g.27161281C= NCBI36
NG_012199.1:g.3167C=
NG_046849.1:g.11343C=
NG_012199.2:g.3167C=

Transcript Alleles

HGVS Amino-acid change
ENST00000380320.9:c.2558-82C= MANE Select ENSP00000369677.4:n.2558-82C=
ENST00000380320.8:c.2558-82C= ENSP00000369677.4:n.2558-82C=
ENST00000433140.1:c.550-82C=
NM_007046.3:c.2558-82C= NP_008977.1:n.2558-82C=
XM_006711928.2:c.2558-82C= XP_006711991.1:n.2558-82C=
NM_007046.4:c.2558-82C= MANE Select NP_008977.1:n.2558-82C=