Canonical Allele Identifier: CA420897057

Gene: ECM1

Linked Data

• MyVariant Identifiers: chr1:g.150483362T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150510886T>G , CM000663.2:g.150510886T>G	GRCh38
NC_000001.10:g.150483362T>G , CM000663.1:g.150483362T>G	GRCh37
NC_000001.9:g.148749986T>G	NCBI36
NG_012062.1:g.7876T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369047.9:c.396T>G MANE Select	ENSP00000358043.4:p.Ala132=
ENST00000346569.6:c.396T>G	ENSP00000271630.6:p.Ala132=
ENST00000369047.8:c.396T>G	ENSP00000358043.4:p.Ala132=
ENST00000369049.8:c.477T>G	ENSP00000358045.4:p.Ala159=
ENST00000470432.5:n.1495T>G
ENST00000498579.5:n.683T>G
NM_001202858.1:c.477T>G	NP_001189787.1:p.Ala159=
NM_004425.3:c.396T>G	NP_004416.2:p.Ala132=
NM_022664.2:c.396T>G	NP_073155.2:p.Ala132=
NM_004425.4:c.396T>G MANE Select	NP_004416.2:p.Ala132=
NM_001202858.2:c.477T>G	NP_001189787.1:p.Ala159=
NM_022664.3:c.396T>G	NP_073155.2:p.Ala132=