Canonical Allele Identifier: CA425382200

Gene: EMILIN1

Linked Data

• MyVariant Identifiers: chr2:g.27308092C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27085224C>T , CM000664.2:g.27085224C>T	GRCh38
NC_000002.11:g.27308092C>T , CM000664.1:g.27308092C>T	GRCh37
NC_000002.10:g.27161596C>T	NCBI36
NG_012199.1:g.3482C>T
NG_046849.1:g.11658C>T
NG_012199.2:g.3482C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380320.9:c.2640C>T MANE Select	ENSP00000369677.4:p.Pro880=
ENST00000380320.8:c.2640C>T	ENSP00000369677.4:p.Pro880=
ENST00000433140.1:c.632C>T
NM_007046.3:c.2640C>T	NP_008977.1:p.Pro880=
XM_006711928.2:c.2575+216C>T	XP_006711991.1:n.2575+216C>T
NM_007046.4:c.2640C>T MANE Select	NP_008977.1:p.Pro880=