Canonical Allele Identifier: CA425382039

Gene: EMILIN1

Linked Data

• MyVariant Identifiers: chr2:g.27307869T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27085001T>A , CM000664.2:g.27085001T>A	GRCh38
NC_000002.11:g.27307869T>A , CM000664.1:g.27307869T>A	GRCh37
NC_000002.10:g.27161373T>A	NCBI36
NG_012199.1:g.3259T>A
NG_046849.1:g.11435T>A
NG_012199.2:g.3259T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380320.9:c.2568T>A MANE Select	ENSP00000369677.4:p.Gly856=
ENST00000380320.8:c.2568T>A	ENSP00000369677.4:p.Gly856=
ENST00000433140.1:c.560T>A
NM_007046.3:c.2568T>A	NP_008977.1:p.Gly856=
XM_006711928.2:c.2568T>A	XP_006711991.1:p.Gly856=
NM_007046.4:c.2568T>A MANE Select	NP_008977.1:p.Gly856=