Canonical Allele Identifier: CA1240109497
Gene: EMILIN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27084840A= , CM000664.2:g.27084840A= GRCh38
NC_000002.11:g.27307708A= , CM000664.1:g.27307708A= GRCh37
NC_000002.10:g.27161212A= NCBI36
NG_012199.1:g.3098A=
NG_046849.1:g.11274A=
NG_012199.2:g.3098A=

Transcript Alleles

HGVS Amino-acid change
ENST00000380320.9:c.2558-151A= MANE Select ENSP00000369677.4:n.2558-151A=
ENST00000380320.8:c.2558-151A= ENSP00000369677.4:n.2558-151A=
ENST00000433140.1:c.550-151A=
NM_007046.3:c.2558-151A= NP_008977.1:n.2558-151A=
XM_006711928.2:c.2558-151A= XP_006711991.1:n.2558-151A=
NM_007046.4:c.2558-151A= MANE Select NP_008977.1:n.2558-151A=