Canonical Allele Identifier: CA1694877512

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24291886_24291887delinsCT , CM000669.2:g.24291886_24291887delinsCT	GRCh38
NC_000007.13:g.24331505_24331506delinsCT , CM000669.1:g.24331505_24331506delinsCT	GRCh37
NC_000007.12:g.24298030_24298031delinsCT	NCBI36
NG_016148.1:g.12699_12700delinsCT

Transcript Alleles

HGVS	Amino-acid Change
XM_017012910.1:c.41+27470_41+27471delinsAG	XP_016868399.1:n.41+27470_41+27471delinsAG
XM_017012911.1:c.41+27470_41+27471delinsAG	XP_016868400.1:n.41+27470_41+27471delinsAG
XR_001745121.1:n.473+27470_473+27471delinsAG
XR_001745122.1:n.345-94858_345-94857delinsAG
XR_001745123.1:n.473+27470_473+27471delinsAG
XR_001745124.1:n.473+27470_473+27471delinsAG
XR_001745125.1:n.473+27470_473+27471delinsAG
XR_001745126.1:n.473+27470_473+27471delinsAG
XR_001745127.1:n.345-36188_345-36187delinsAG
XR_001745129.1:n.473+27470_473+27471delinsAG
XR_001745130.1:n.473+27470_473+27471delinsAG
XR_001745131.1:n.473+27470_473+27471delinsAG
XR_001745132.1:n.473+27470_473+27471delinsAG