Canonical Allele Identifier: CA420897058

Gene: ECM1

Linked Data

• MyVariant Identifiers: chr1:g.150483365A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150510889A>C , CM000663.2:g.150510889A>C	GRCh38
NC_000001.10:g.150483365A>C , CM000663.1:g.150483365A>C	GRCh37
NC_000001.9:g.148749989A>C	NCBI36
NG_012062.1:g.7879A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369047.9:c.399A>C MANE Select	ENSP00000358043.4:p.Pro133=
ENST00000346569.6:c.399A>C	ENSP00000271630.6:p.Pro133=
ENST00000369047.8:c.399A>C	ENSP00000358043.4:p.Pro133=
ENST00000369049.8:c.480A>C	ENSP00000358045.4:p.Pro160=
ENST00000470432.5:n.1498A>C
ENST00000498579.5:n.686A>C
NM_001202858.1:c.480A>C	NP_001189787.1:p.Pro160=
NM_004425.3:c.399A>C	NP_004416.2:p.Pro133=
NM_022664.2:c.399A>C	NP_073155.2:p.Pro133=
NM_004425.4:c.399A>C MANE Select	NP_004416.2:p.Pro133=
NM_001202858.2:c.480A>C	NP_001189787.1:p.Pro160=
NM_022664.3:c.399A>C	NP_073155.2:p.Pro133=