Canonical Allele Identifier: CA1694873180

Gene:

Linked Data

• dbSNP Id: rs1787214903

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24283309_24283310del , CM000669.2:g.24283309_24283310del	GRCh38
NC_000007.13:g.24322928_24322929del , CM000669.1:g.24322928_24322929del	GRCh37
NC_000007.12:g.24289453_24289454del	NCBI36
NG_016148.1:g.4122_4123del

Transcript Alleles

HGVS	Amino-acid Change
XM_017012910.1:c.42-27611_42-27610del	XP_016868399.1:n.42-27611_42-27610del
XM_017012911.1:c.42-27611_42-27610del	XP_016868400.1:n.42-27611_42-27610del
XR_001745121.1:n.473+36047_473+36048del
XR_001745122.1:n.345-86281_345-86280del
XR_001745123.1:n.473+36047_473+36048del
XR_001745124.1:n.473+36047_473+36048del
XR_001745125.1:n.473+36047_473+36048del
XR_001745126.1:n.473+36047_473+36048del
XR_001745127.1:n.345-27611_345-27610del
XR_001745129.1:n.473+36047_473+36048del
XR_001745130.1:n.473+36047_473+36048del
XR_001745131.1:n.473+36047_473+36048del
XR_001745132.1:n.473+36047_473+36048del