Canonical Allele Identifier: CA601669471

Gene: MMP1 WTAPP1

Linked Data

• gnomAD v2: 11-102661568-CTTTT-C
• MyVariant Identifiers: chr11:g.102661569_102661572del (hg19) ; chr11:g.102790838_102790841del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102790838_102790841del , CM000673.2:g.102790838_102790841del	GRCh38
NC_000011.9:g.102661569_102661572del , CM000673.1:g.102661569_102661572del	GRCh37
NC_000011.8:g.102166779_102166782del	NCBI36
NG_011740.1:g.12395_12398del
NG_011740.2:g.12395_12398del

Transcript Alleles

HGVS	Amino-acid change
ENST00000315274.7:c.1197-35_1197-32del (MMP1) MANE Select	ENSP00000322788.6:n.1197-35_1197-32del
ENST00000680179.1:n.375-35_375-32del (MMP1)
ENST00000681445.1:n.371-35_371-32del (MMP1)
ENST00000681643.1:n.397-35_397-32del (MMP1)
ENST00000315274.6:c.1197-35_1197-32del (MMP1)	ENSP00000322788.6:n.1197-35_1197-32del
ENST00000371455.7:n.325-7186_325-7183del (WTAPP1)
ENST00000525739.6:n.390-2307_390-2304del (WTAPP1)
ENST00000544704.1:n.344+6774_344+6777del (WTAPP1)
NM_001145938.1:c.999-35_999-32del (MMP1)	NP_001139410.1:n.999-35_999-32del
NM_002421.3:c.1197-35_1197-32del (MMP1)	NP_002412.1:n.1197-35_1197-32del
NR_038390.1:n.390-2307_390-2304del (WTAPP1)
NM_002421.4:c.1197-35_1197-32del (MMP1) MANE Select	NP_002412.1:n.1197-35_1197-32del
NM_001145938.2:c.999-35_999-32del (MMP1)	NP_001139410.1:n.999-35_999-32del