Canonical Allele Identifier: CA2615724712

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102790153_102790156del , CM000673.2:g.102790153_102790156del GRCh38
NC_000011.9:g.102660884_102660887del , CM000673.1:g.102660884_102660887del GRCh37
NC_000011.8:g.102166094_102166097del NCBI36
NG_011740.1:g.13080_13083del
NG_011740.2:g.13080_13083del

Transcript Alleles

HGVS Amino-acid change
ENST00000315274.7:c.*256_*259del (MMP1) MANE Select ENSP00000322788.6:n.*256_*259del
ENST00000680179.1:n.844_847del (MMP1)
ENST00000681445.1:n.840_843del (MMP1)
ENST00000681643.1:n.866_869del (MMP1)
ENST00000315274.6:c.*256_*259del (MMP1) ENSP00000322788.6:n.*256_*259del
ENST00000371455.7:n.325-7871_325-7868del (WTAPP1)
ENST00000525739.6:n.390-2992_390-2989del (WTAPP1)
ENST00000544704.1:n.344+6089_344+6092del (WTAPP1)
NM_001145938.1:c.*256_*259del (MMP1) NP_001139410.1:n.*256_*259del
NM_002421.3:c.*256_*259del (MMP1) NP_002412.1:n.*256_*259del
NR_038390.1:n.390-2992_390-2989del (WTAPP1)
NM_002421.4:c.*256_*259del (MMP1) MANE Select NP_002412.1:n.*256_*259del
NM_001145938.2:c.*256_*259del (MMP1) NP_001139410.1:n.*256_*259del