Canonical Allele Identifier: CA836922190

Gene:

Linked Data

• dbSNP Id: rs1295010158
• MyVariant Identifiers: chr7:g.24323494_24323497del (hg19) ; chr7:g.24283875_24283878del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24283878_24283881del , CM000669.2:g.24283878_24283881del	GRCh38
NC_000007.13:g.24323497_24323500del , CM000669.1:g.24323497_24323500del	GRCh37
NC_000007.12:g.24290022_24290025del	NCBI36
NG_016148.1:g.4691_4694del

Transcript Alleles

HGVS	Amino-acid change
XM_017012910.1:c.42-28179_42-28176del	XP_016868399.1:n.42-28179_42-28176del
XM_017012911.1:c.42-28179_42-28176del	XP_016868400.1:n.42-28179_42-28176del
XR_001745121.1:n.473+35479_473+35482del
XR_001745122.1:n.345-86849_345-86846del
XR_001745123.1:n.473+35479_473+35482del
XR_001745124.1:n.473+35479_473+35482del
XR_001745125.1:n.473+35479_473+35482del
XR_001745126.1:n.473+35479_473+35482del
XR_001745127.1:n.345-28179_345-28176del
XR_001745129.1:n.473+35479_473+35482del
XR_001745130.1:n.473+35479_473+35482del
XR_001745131.1:n.473+35479_473+35482del
XR_001745132.1:n.473+35479_473+35482del