Canonical Allele Identifier: CA1099424071
Gene:

Linked Data

dbSNP Id: rs1787235661

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24283650_24283656del , CM000669.2:g.24283650_24283656del GRCh38
NC_000007.13:g.24323269_24323275del , CM000669.1:g.24323269_24323275del GRCh37
NC_000007.12:g.24289794_24289800del NCBI36
NG_016148.1:g.4463_4469del

Transcript Alleles

HGVS Amino-acid change
XM_017012910.1:c.42-27955_42-27949del XP_016868399.1:n.42-27955_42-27949del
XM_017012911.1:c.42-27955_42-27949del XP_016868400.1:n.42-27955_42-27949del
XR_001745121.1:n.473+35703_473+35709del
XR_001745122.1:n.345-86625_345-86619del
XR_001745123.1:n.473+35703_473+35709del
XR_001745124.1:n.473+35703_473+35709del
XR_001745125.1:n.473+35703_473+35709del
XR_001745126.1:n.473+35703_473+35709del
XR_001745127.1:n.345-27955_345-27949del
XR_001745129.1:n.473+35703_473+35709del
XR_001745130.1:n.473+35703_473+35709del
XR_001745131.1:n.473+35703_473+35709del
XR_001745132.1:n.473+35703_473+35709del