Canonical Allele Identifier: CA1694877531

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24291914_24291915delinsTA , CM000669.2:g.24291914_24291915delinsTA	GRCh38
NC_000007.13:g.24331533_24331534delinsTA , CM000669.1:g.24331533_24331534delinsTA	GRCh37
NC_000007.12:g.24298058_24298059delinsTA	NCBI36
NG_016148.1:g.12727_12728delinsTA

Transcript Alleles

HGVS	Amino-acid Change
XM_017012910.1:c.41+27442_41+27443delinsTA	XP_016868399.1:n.41+27442_41+27443delinsTA
XM_017012911.1:c.41+27442_41+27443delinsTA	XP_016868400.1:n.41+27442_41+27443delinsTA
XR_001745121.1:n.473+27442_473+27443delinsTA
XR_001745122.1:n.345-94886_345-94885delinsTA
XR_001745123.1:n.473+27442_473+27443delinsTA
XR_001745124.1:n.473+27442_473+27443delinsTA
XR_001745125.1:n.473+27442_473+27443delinsTA
XR_001745126.1:n.473+27442_473+27443delinsTA
XR_001745127.1:n.345-36216_345-36215delinsTA
XR_001745129.1:n.473+27442_473+27443delinsTA
XR_001745130.1:n.473+27442_473+27443delinsTA
XR_001745131.1:n.473+27442_473+27443delinsTA
XR_001745132.1:n.473+27442_473+27443delinsTA