Canonical Allele Identifier: CA1148441136

Gene: ECM1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150510841C= , CM000663.2:g.150510841C=	GRCh38
NC_000001.10:g.150483317C= , CM000663.1:g.150483317C=	GRCh37
NC_000001.9:g.148749941C=	NCBI36
NG_012062.1:g.7831C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369047.9:c.386-35C= MANE Select	ENSP00000358043.4:n.386-35C=
ENST00000346569.6:c.386-35C=	ENSP00000271630.6:n.386-35C=
ENST00000369047.8:c.386-35C=	ENSP00000358043.4:n.386-35C=
ENST00000369049.8:c.467-35C=	ENSP00000358045.4:n.467-35C=
ENST00000470432.5:n.1450C=
ENST00000498579.5:n.673-35C=
NM_001202858.1:c.467-35C=	NP_001189787.1:n.467-35C=
NM_004425.3:c.386-35C=	NP_004416.2:n.386-35C=
NM_022664.2:c.386-35C=	NP_073155.2:n.386-35C=
XR_922130.1:n.29G=
NM_004425.4:c.386-35C= MANE Select	NP_004416.2:n.386-35C=
NM_001202858.2:c.467-35C=	NP_001189787.1:n.467-35C=
NM_022664.3:c.386-35C=	NP_073155.2:n.386-35C=