Canonical Allele Identifier: CA346156109

Gene: EMILIN1

Linked Data

• MyVariant Identifiers: chr2:g.27308071T>A (hg19) ; chr2:g.27085203T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27085203T>A , CM000664.2:g.27085203T>A	GRCh38
NC_000002.11:g.27308071T>A , CM000664.1:g.27308071T>A	GRCh37
NC_000002.10:g.27161575T>A	NCBI36
NG_012199.1:g.3461T>A
NG_046849.1:g.11637T>A
NG_012199.2:g.3461T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380320.9:c.2619T>A MANE Select	ENSP00000369677.4:p.Phe873Leu
ENST00000380320.8:c.2619T>A	ENSP00000369677.4:p.Phe873Leu
ENST00000433140.1:c.611T>A
NM_007046.3:c.2619T>A	NP_008977.1:p.Phe873Leu
XM_006711928.2:c.2575+195T>A	XP_006711991.1:n.2575+195T>A
NM_007046.4:c.2619T>A MANE Select	NP_008977.1:p.Phe873Leu