Canonical Allele Identifier: CA155828714

Gene:

Linked Data

• dbSNP Id: rs749284003
• gnomAD v2: 7-24322301-TAGA-T
• gnomAD v3: 7-24282682-TAGA-T
• gnomAD v4: 7-24282682-TAGA-T
• MyVariant Identifiers: chr7:g.24322302_24322304del (hg19) ; chr7:g.24282683_24282685del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24282686_24282688del , CM000669.2:g.24282686_24282688del	GRCh38
NC_000007.13:g.24322305_24322307del , CM000669.1:g.24322305_24322307del	GRCh37
NC_000007.12:g.24288830_24288832del	NCBI36
NG_016148.1:g.3499_3501del

Transcript Alleles

HGVS	Amino-acid change
XM_017012910.1:c.42-26986_42-26984del	XP_016868399.1:n.42-26986_42-26984del
XM_017012911.1:c.42-26986_42-26984del	XP_016868400.1:n.42-26986_42-26984del
XR_001745121.1:n.473+36672_473+36674del
XR_001745122.1:n.345-85656_345-85654del
XR_001745123.1:n.473+36672_473+36674del
XR_001745124.1:n.473+36672_473+36674del
XR_001745125.1:n.473+36672_473+36674del
XR_001745126.1:n.473+36672_473+36674del
XR_001745127.1:n.345-26986_345-26984del
XR_001745129.1:n.473+36672_473+36674del
XR_001745130.1:n.473+36672_473+36674del
XR_001745131.1:n.473+36672_473+36674del
XR_001745132.1:n.473+36672_473+36674del