Canonical Allele Identifier: CA2615724435

Gene: MMP1 WTAPP1

Linked Data

• gnomAD v4: 11-102789999-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102789999C>A , CM000673.2:g.102789999C>A	GRCh38
NC_000011.9:g.102660730C>A , CM000673.1:g.102660730C>A	GRCh37
NC_000011.8:g.102165940C>A	NCBI36
NG_011740.1:g.13237G>T
NG_011740.2:g.13237G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000315274.7:c.*413G>T (MMP1) MANE Select	ENSP00000322788.6:n.*413G>T
ENST00000680179.1:n.1001G>T (MMP1)
ENST00000681445.1:n.997G>T (MMP1)
ENST00000681643.1:n.1023G>T (MMP1)
ENST00000315274.6:c.*413G>T (MMP1)	ENSP00000322788.6:n.*413G>T
ENST00000371455.7:n.325-8025C>A (WTAPP1)
ENST00000525739.6:n.390-3146C>A (WTAPP1)
ENST00000544704.1:n.344+5935C>A (WTAPP1)
NM_001145938.1:c.*413G>T (MMP1)	NP_001139410.1:n.*413G>T
NM_002421.3:c.*413G>T (MMP1)	NP_002412.1:n.*413G>T
NR_038390.1:n.390-3146C>A (WTAPP1)
NM_002421.4:c.*413G>T (MMP1) MANE Select	NP_002412.1:n.*413G>T
NM_001145938.2:c.*413G>T (MMP1)	NP_001139410.1:n.*413G>T