Canonical Allele Identifier: CA836921971

Gene:

Linked Data

• dbSNP Id: rs1229474069
• MyVariant Identifiers: chr7:g.24323177_24323188del (hg19) ; chr7:g.24283558_24283569del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24283559_24283570del , CM000669.2:g.24283559_24283570del	GRCh38
NC_000007.13:g.24323178_24323189del , CM000669.1:g.24323178_24323189del	GRCh37
NC_000007.12:g.24289703_24289714del	NCBI36
NG_016148.1:g.4372_4383del

Transcript Alleles

HGVS	Amino-acid Change
XM_017012910.1:c.42-27870_42-27859del	XP_016868399.1:n.42-27870_42-27859del
XM_017012911.1:c.42-27870_42-27859del	XP_016868400.1:n.42-27870_42-27859del
XR_001745121.1:n.473+35788_473+35799del
XR_001745122.1:n.345-86540_345-86529del
XR_001745123.1:n.473+35788_473+35799del
XR_001745124.1:n.473+35788_473+35799del
XR_001745125.1:n.473+35788_473+35799del
XR_001745126.1:n.473+35788_473+35799del
XR_001745127.1:n.345-27870_345-27859del
XR_001745129.1:n.473+35788_473+35799del
XR_001745130.1:n.473+35788_473+35799del
XR_001745131.1:n.473+35788_473+35799del
XR_001745132.1:n.473+35788_473+35799del