Canonical Allele Identifier: CA836921905

Gene:

Linked Data

• dbSNP Id: rs1239206477
• gnomAD v3: 7-24283374-TAA-T
• gnomAD v4: 7-24283374-TAA-T
• MyVariant Identifiers: chr7:g.24322994_24322995del (hg19) ; chr7:g.24283375_24283376del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24283377_24283378del , CM000669.2:g.24283377_24283378del	GRCh38
NC_000007.13:g.24322996_24322997del , CM000669.1:g.24322996_24322997del	GRCh37
NC_000007.12:g.24289521_24289522del	NCBI36
NG_016148.1:g.4190_4191del

Transcript Alleles

HGVS	Amino-acid Change
XM_017012910.1:c.42-27677_42-27676del	XP_016868399.1:n.42-27677_42-27676del
XM_017012911.1:c.42-27677_42-27676del	XP_016868400.1:n.42-27677_42-27676del
XR_001745121.1:n.473+35981_473+35982del
XR_001745122.1:n.345-86347_345-86346del
XR_001745123.1:n.473+35981_473+35982del
XR_001745124.1:n.473+35981_473+35982del
XR_001745125.1:n.473+35981_473+35982del
XR_001745126.1:n.473+35981_473+35982del
XR_001745127.1:n.345-27677_345-27676del
XR_001745129.1:n.473+35981_473+35982del
XR_001745130.1:n.473+35981_473+35982del
XR_001745131.1:n.473+35981_473+35982del
XR_001745132.1:n.473+35981_473+35982del