Canonical Allele Identifier: CA1694872892

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24282682_24282685delinsTAGA , CM000669.2:g.24282682_24282685delinsTAGA	GRCh38
NC_000007.13:g.24322301_24322304delinsTAGA , CM000669.1:g.24322301_24322304delinsTAGA	GRCh37
NC_000007.12:g.24288826_24288829delinsTAGA	NCBI36
NG_016148.1:g.3495_3498delinsTAGA

Transcript Alleles

HGVS	Amino-acid change
XM_017012910.1:c.42-26986_42-26983delinsTCTA	XP_016868399.1:n.42-26986_42-26983delinsTCTA
XM_017012911.1:c.42-26986_42-26983delinsTCTA	XP_016868400.1:n.42-26986_42-26983delinsTCTA
XR_001745121.1:n.473+36672_473+36675delinsTCTA
XR_001745122.1:n.345-85656_345-85653delinsTCTA
XR_001745123.1:n.473+36672_473+36675delinsTCTA
XR_001745124.1:n.473+36672_473+36675delinsTCTA
XR_001745125.1:n.473+36672_473+36675delinsTCTA
XR_001745126.1:n.473+36672_473+36675delinsTCTA
XR_001745127.1:n.345-26986_345-26983delinsTCTA
XR_001745129.1:n.473+36672_473+36675delinsTCTA
XR_001745130.1:n.473+36672_473+36675delinsTCTA
XR_001745131.1:n.473+36672_473+36675delinsTCTA
XR_001745132.1:n.473+36672_473+36675delinsTCTA