Canonical Allele Identifier: CA1694873184

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24283338_24283339delinsCA , CM000669.2:g.24283338_24283339delinsCA	GRCh38
NC_000007.13:g.24322957_24322958delinsCA , CM000669.1:g.24322957_24322958delinsCA	GRCh37
NC_000007.12:g.24289482_24289483delinsCA	NCBI36
NG_016148.1:g.4151_4152delinsCA

Transcript Alleles

HGVS	Amino-acid Change
XM_017012910.1:c.42-27640_42-27639delinsTG	XP_016868399.1:n.42-27640_42-27639delinsTG
XM_017012911.1:c.42-27640_42-27639delinsTG	XP_016868400.1:n.42-27640_42-27639delinsTG
XR_001745121.1:n.473+36018_473+36019delinsTG
XR_001745122.1:n.345-86310_345-86309delinsTG
XR_001745123.1:n.473+36018_473+36019delinsTG
XR_001745124.1:n.473+36018_473+36019delinsTG
XR_001745125.1:n.473+36018_473+36019delinsTG
XR_001745126.1:n.473+36018_473+36019delinsTG
XR_001745127.1:n.345-27640_345-27639delinsTG
XR_001745129.1:n.473+36018_473+36019delinsTG
XR_001745130.1:n.473+36018_473+36019delinsTG
XR_001745131.1:n.473+36018_473+36019delinsTG
XR_001745132.1:n.473+36018_473+36019delinsTG