Canonical Allele Identifier: CA2615724906

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102790260_102790261insGGA , CM000673.2:g.102790260_102790261insGGA GRCh38
NC_000011.9:g.102660991_102660992insGGA , CM000673.1:g.102660991_102660992insGGA GRCh37
NC_000011.8:g.102166201_102166202insGGA NCBI36
NG_011740.1:g.12975_12976insTCC
NG_011740.2:g.12975_12976insTCC

Transcript Alleles

HGVS Amino-acid change
ENST00000315274.7:c.*151_*152insTCC (MMP1) MANE Select ENSP00000322788.6:n.*151_*152insTCC
ENST00000680179.1:n.739_740insTCC (MMP1)
ENST00000681445.1:n.735_736insTCC (MMP1)
ENST00000681643.1:n.761_762insTCC (MMP1)
ENST00000315274.6:c.*151_*152insTCC (MMP1) ENSP00000322788.6:n.*151_*152insTCC
ENST00000371455.7:n.325-7764_325-7763insGGA (WTAPP1)
ENST00000525739.6:n.390-2885_390-2884insGGA (WTAPP1)
ENST00000544704.1:n.344+6196_344+6197insGGA (WTAPP1)
NM_001145938.1:c.*151_*152insTCC (MMP1) NP_001139410.1:n.*151_*152insTCC
NM_002421.3:c.*151_*152insTCC (MMP1) NP_002412.1:n.*151_*152insTCC
NR_038390.1:n.390-2885_390-2884insGGA (WTAPP1)
NM_002421.4:c.*151_*152insTCC (MMP1) MANE Select NP_002412.1:n.*151_*152insTCC
NM_001145938.2:c.*151_*152insTCC (MMP1) NP_001139410.1:n.*151_*152insTCC