Canonical Allele Identifier: CA2576702676

Gene: EMILIN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27085062A>G , CM000664.2:g.27085062A>G	GRCh38
NC_000002.11:g.27307930A>G , CM000664.1:g.27307930A>G	GRCh37
NC_000002.10:g.27161434A>G	NCBI36
NG_012199.1:g.3320A>G
NG_046849.1:g.11496A>G
NG_012199.2:g.3320A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380320.9:c.2575+54A>G MANE Select	ENSP00000369677.4:n.2575+54A>G
ENST00000380320.8:c.2575+54A>G	ENSP00000369677.4:n.2575+54A>G
ENST00000433140.1:c.567+54A>G
NM_007046.3:c.2575+54A>G	NP_008977.1:n.2575+54A>G
XM_006711928.2:c.2575+54A>G	XP_006711991.1:n.2575+54A>G
NM_007046.4:c.2575+54A>G MANE Select	NP_008977.1:n.2575+54A>G