Canonical Allele Identifier: CA155828858

Gene:

Linked Data

• dbSNP Id: rs958931463
• gnomAD v3: 7-24283788-G-GGGTT
• gnomAD v4: 7-24283788-G-GGGTT
• MyVariant Identifiers: chr7:g.24323407_24323408insGGTT (hg19) ; chr7:g.24283788_24283789insGGTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24283792_24283795dup , CM000669.2:g.24283792_24283795dup	GRCh38
NC_000007.13:g.24323411_24323414dup , CM000669.1:g.24323411_24323414dup	GRCh37
NC_000007.12:g.24289936_24289939dup	NCBI36
NG_016148.1:g.4605_4608dup

Transcript Alleles

HGVS	Amino-acid Change
XM_017012910.1:c.42-28093_42-28090dup	XP_016868399.1:n.42-28093_42-28090dup
XM_017012911.1:c.42-28093_42-28090dup	XP_016868400.1:n.42-28093_42-28090dup
XR_001745121.1:n.473+35565_473+35568dup
XR_001745122.1:n.345-86763_345-86760dup
XR_001745123.1:n.473+35565_473+35568dup
XR_001745124.1:n.473+35565_473+35568dup
XR_001745125.1:n.473+35565_473+35568dup
XR_001745126.1:n.473+35565_473+35568dup
XR_001745127.1:n.345-28093_345-28090dup
XR_001745129.1:n.473+35565_473+35568dup
XR_001745130.1:n.473+35565_473+35568dup
XR_001745131.1:n.473+35565_473+35568dup
XR_001745132.1:n.473+35565_473+35568dup