Canonical Allele Identifier: CA2497334622

Gene: MMP1 WTAPP1

Linked Data

• dbSNP Id: rs1858010504

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102790903_102790904insG , CM000673.2:g.102790903_102790904insG	GRCh38
NC_000011.9:g.102661634_102661635insG , CM000673.1:g.102661634_102661635insG	GRCh37
NC_000011.8:g.102166844_102166845insG	NCBI36
NG_011740.1:g.12332_12333insC
NG_011740.2:g.12332_12333insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315274.7:c.1197-98_1197-97insC (MMP1) MANE Select	ENSP00000322788.6:n.1197-98_1197-97insC
ENST00000680179.1:n.375-98_375-97insC (MMP1)
ENST00000681445.1:n.371-98_371-97insC (MMP1)
ENST00000681643.1:n.397-98_397-97insC (MMP1)
ENST00000315274.6:c.1197-98_1197-97insC (MMP1)	ENSP00000322788.6:n.1197-98_1197-97insC
ENST00000371455.7:n.325-7121_325-7120insG (WTAPP1)
ENST00000525739.6:n.390-2242_390-2241insG (WTAPP1)
ENST00000544704.1:n.344+6839_344+6840insG (WTAPP1)
NM_001145938.1:c.999-98_999-97insC (MMP1)	NP_001139410.1:n.999-98_999-97insC
NM_002421.3:c.1197-98_1197-97insC (MMP1)	NP_002412.1:n.1197-98_1197-97insC
NR_038390.1:n.390-2242_390-2241insG (WTAPP1)
NM_002421.4:c.1197-98_1197-97insC (MMP1) MANE Select	NP_002412.1:n.1197-98_1197-97insC
NM_001145938.2:c.999-98_999-97insC (MMP1)	NP_001139410.1:n.999-98_999-97insC