Canonical Allele Identifier: CA2615724608

Gene: MMP1 WTAPP1

Linked Data

• gnomAD v4: 11-102790120-TCAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102790122_102790124del , CM000673.2:g.102790122_102790124del	GRCh38
NC_000011.9:g.102660853_102660855del , CM000673.1:g.102660853_102660855del	GRCh37
NC_000011.8:g.102166063_102166065del	NCBI36
NG_011740.1:g.13113_13115del
NG_011740.2:g.13113_13115del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315274.7:c.*289_*291del (MMP1) MANE Select	ENSP00000322788.6:n.*289_*291del
ENST00000680179.1:n.877_879del (MMP1)
ENST00000681445.1:n.873_875del (MMP1)
ENST00000681643.1:n.899_901del (MMP1)
ENST00000315274.6:c.*289_*291del (MMP1)	ENSP00000322788.6:n.*289_*291del
ENST00000371455.7:n.325-7902_325-7900del (WTAPP1)
ENST00000525739.6:n.390-3023_390-3021del (WTAPP1)
ENST00000544704.1:n.344+6058_344+6060del (WTAPP1)
NM_001145938.1:c.*289_*291del (MMP1)	NP_001139410.1:n.*289_*291del
NM_002421.3:c.*289_*291del (MMP1)	NP_002412.1:n.*289_*291del
NR_038390.1:n.390-3023_390-3021del (WTAPP1)
NM_002421.4:c.*289_*291del (MMP1) MANE Select	NP_002412.1:n.*289_*291del
NM_001145938.2:c.*289_*291del (MMP1)	NP_001139410.1:n.*289_*291del