Canonical Allele Identifier: CA1694873285

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24283534_24283535delinsGA , CM000669.2:g.24283534_24283535delinsGA	GRCh38
NC_000007.13:g.24323153_24323154delinsGA , CM000669.1:g.24323153_24323154delinsGA	GRCh37
NC_000007.12:g.24289678_24289679delinsGA	NCBI36
NG_016148.1:g.4347_4348delinsGA

Transcript Alleles

HGVS	Amino-acid Change
XM_017012910.1:c.42-27836_42-27835delinsTC	XP_016868399.1:n.42-27836_42-27835delinsTC
XM_017012911.1:c.42-27836_42-27835delinsTC	XP_016868400.1:n.42-27836_42-27835delinsTC
XR_001745121.1:n.473+35822_473+35823delinsTC
XR_001745122.1:n.345-86506_345-86505delinsTC
XR_001745123.1:n.473+35822_473+35823delinsTC
XR_001745124.1:n.473+35822_473+35823delinsTC
XR_001745125.1:n.473+35822_473+35823delinsTC
XR_001745126.1:n.473+35822_473+35823delinsTC
XR_001745127.1:n.345-27836_345-27835delinsTC
XR_001745129.1:n.473+35822_473+35823delinsTC
XR_001745130.1:n.473+35822_473+35823delinsTC
XR_001745131.1:n.473+35822_473+35823delinsTC
XR_001745132.1:n.473+35822_473+35823delinsTC