Canonical Allele Identifier: CA1240109696

Gene: EMILIN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27085241C= , CM000664.2:g.27085241C=	GRCh38
NC_000002.11:g.27308109C= , CM000664.1:g.27308109C=	GRCh37
NC_000002.10:g.27161613C=	NCBI36
NG_012199.1:g.3499C=
NG_046849.1:g.11675C=
NG_012199.2:g.3499C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380320.9:c.2657C= MANE Select	ENSP00000369677.4:p.Thr886=
ENST00000380320.8:c.2657C=	ENSP00000369677.4:p.Thr886=
ENST00000433140.1:c.649C=
NM_007046.3:c.2657C=	NP_008977.1:p.Thr886=
XM_006711928.2:c.2575+233C=	XP_006711991.1:n.2575+233C=
NM_007046.4:c.2657C= MANE Select	NP_008977.1:p.Thr886=