Canonical Allele Identifier: CA1099424150
Gene:

Linked Data

dbSNP Id: rs1787246621

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24283884_24283891del , CM000669.2:g.24283884_24283891del GRCh38
NC_000007.13:g.24323503_24323510del , CM000669.1:g.24323503_24323510del GRCh37
NC_000007.12:g.24290028_24290035del NCBI36
NG_016148.1:g.4697_4704del

Transcript Alleles

HGVS Amino-acid change
XM_017012910.1:c.42-28189_42-28182del XP_016868399.1:n.42-28189_42-28182del
XM_017012911.1:c.42-28189_42-28182del XP_016868400.1:n.42-28189_42-28182del
XR_001745121.1:n.473+35469_473+35476del
XR_001745122.1:n.345-86859_345-86852del
XR_001745123.1:n.473+35469_473+35476del
XR_001745124.1:n.473+35469_473+35476del
XR_001745125.1:n.473+35469_473+35476del
XR_001745126.1:n.473+35469_473+35476del
XR_001745127.1:n.345-28189_345-28182del
XR_001745129.1:n.473+35469_473+35476del
XR_001745130.1:n.473+35469_473+35476del
XR_001745131.1:n.473+35469_473+35476del
XR_001745132.1:n.473+35469_473+35476del