Canonical Allele Identifier: CA2497334619

Gene: MMP1 WTAPP1

Linked Data

• dbSNP Id: rs1858007817

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102790828_102790835del , CM000673.2:g.102790828_102790835del	GRCh38
NC_000011.9:g.102661559_102661566del , CM000673.1:g.102661559_102661566del	GRCh37
NC_000011.8:g.102166769_102166776del	NCBI36
NG_011740.1:g.12404_12411del
NG_011740.2:g.12404_12411del

Transcript Alleles

HGVS	Amino-acid change
ENST00000315274.7:c.1197-26_1197-19del (MMP1) MANE Select	ENSP00000322788.6:n.1197-26_1197-19del
ENST00000680179.1:n.375-26_375-19del (MMP1)
ENST00000681445.1:n.371-26_371-19del (MMP1)
ENST00000681643.1:n.397-26_397-19del (MMP1)
ENST00000315274.6:c.1197-26_1197-19del (MMP1)	ENSP00000322788.6:n.1197-26_1197-19del
ENST00000371455.7:n.325-7196_325-7189del (WTAPP1)
ENST00000525739.6:n.390-2317_390-2310del (WTAPP1)
ENST00000544704.1:n.344+6764_344+6771del (WTAPP1)
NM_001145938.1:c.999-26_999-19del (MMP1)	NP_001139410.1:n.999-26_999-19del
NM_002421.3:c.1197-26_1197-19del (MMP1)	NP_002412.1:n.1197-26_1197-19del
NR_038390.1:n.390-2317_390-2310del (WTAPP1)
NM_002421.4:c.1197-26_1197-19del (MMP1) MANE Select	NP_002412.1:n.1197-26_1197-19del
NM_001145938.2:c.999-26_999-19del (MMP1)	NP_001139410.1:n.999-26_999-19del