Canonical Allele Identifier: CA1143760519

Gene: ECM1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150510882C= , CM000663.2:g.150510882C=	GRCh38
NC_000001.10:g.150483358C= , CM000663.1:g.150483358C=	GRCh37
NC_000001.9:g.148749982C=	NCBI36
NG_012062.1:g.7872C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369047.9:c.392C= MANE Select	ENSP00000358043.4:p.Pro131=
ENST00000346569.6:c.392C=	ENSP00000271630.6:p.Pro131=
ENST00000369047.8:c.392C=	ENSP00000358043.4:p.Pro131=
ENST00000369049.8:c.473C=	ENSP00000358045.4:p.Pro158=
ENST00000470432.5:n.1491C=
ENST00000498579.5:n.679C=
NM_001202858.1:c.473C=	NP_001189787.1:p.Pro158=
NM_004425.3:c.392C=	NP_004416.2:p.Pro131=
NM_022664.2:c.392C=	NP_073155.2:p.Pro131=
NM_004425.4:c.392C= MANE Select	NP_004416.2:p.Pro131=
NM_001202858.2:c.473C=	NP_001189787.1:p.Pro158=
NM_022664.3:c.392C=	NP_073155.2:p.Pro131=