Canonical Allele Identifier: CA917965003

Gene:

Linked Data

• dbSNP Id: rs1041422397

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24283425del , CM000669.2:g.24283425del	GRCh38
NC_000007.13:g.24323044del , CM000669.1:g.24323044del	GRCh37
NC_000007.12:g.24289569del	NCBI36
NG_016148.1:g.4238del

Transcript Alleles

HGVS	Amino-acid Change
XM_017012910.1:c.42-27722del	XP_016868399.1:n.42-27722del
XM_017012911.1:c.42-27722del	XP_016868400.1:n.42-27722del
XR_001745121.1:n.473+35936del
XR_001745122.1:n.345-86392del
XR_001745123.1:n.473+35936del
XR_001745124.1:n.473+35936del
XR_001745125.1:n.473+35936del
XR_001745126.1:n.473+35936del
XR_001745127.1:n.345-27722del
XR_001745129.1:n.473+35936del
XR_001745130.1:n.473+35936del
XR_001745131.1:n.473+35936del
XR_001745132.1:n.473+35936del