Canonical Allele Identifier: CA1694873313

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24283579_24283580delinsCG , CM000669.2:g.24283579_24283580delinsCG	GRCh38
NC_000007.13:g.24323198_24323199delinsCG , CM000669.1:g.24323198_24323199delinsCG	GRCh37
NC_000007.12:g.24289723_24289724delinsCG	NCBI36
NG_016148.1:g.4392_4393delinsCG

Transcript Alleles

HGVS	Amino-acid change
XM_017012910.1:c.42-27881_42-27880delinsCG	XP_016868399.1:n.42-27881_42-27880delinsC...
XM_017012911.1:c.42-27881_42-27880delinsCG	XP_016868400.1:n.42-27881_42-27880delinsC...
XR_001745121.1:n.473+35777_473+35778delinsCG
XR_001745122.1:n.345-86551_345-86550delinsCG
XR_001745123.1:n.473+35777_473+35778delinsCG
XR_001745124.1:n.473+35777_473+35778delinsCG
XR_001745125.1:n.473+35777_473+35778delinsCG
XR_001745126.1:n.473+35777_473+35778delinsCG
XR_001745127.1:n.345-27881_345-27880delinsCG
XR_001745129.1:n.473+35777_473+35778delinsCG
XR_001745130.1:n.473+35777_473+35778delinsCG
XR_001745131.1:n.473+35777_473+35778delinsCG
XR_001745132.1:n.473+35777_473+35778delinsCG