Canonical Allele Identifier: CA2724604489

Linked Data

dbSNP Id: rs1035718049

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102789739_102789740insCCCCCC , CM000673.2:g.102789739_102789740insCCCCCC GRCh38
NC_000011.9:g.102660470_102660471insCCCCCC , CM000673.1:g.102660470_102660471insCCCCCC GRCh37
NC_000011.8:g.102165680_102165681insCCCCCC NCBI36
NG_011740.1:g.13501_13502insGGGGGG
NG_011740.2:g.13501_13502insGGGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000680179.1:n.1265_1266insGGGGGG (MMP1)
ENST00000681445.1:n.1261_1262insGGGGGG (MMP1)
ENST00000681643.1:n.1287_1288insGGGGGG (MMP1)
ENST00000371455.7:n.325-8285_325-8284insCCCCCC (WTAPP1)
ENST00000525739.6:n.390-3406_390-3405insCCCCCC (WTAPP1)
ENST00000544704.1:n.344+5675_344+5676insCCCCCC (WTAPP1)
NR_038390.1:n.390-3406_390-3405insCCCCCC (WTAPP1)