Canonical Allele Identifier: CA1694873176

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24283308_24283310delinsGTT , CM000669.2:g.24283308_24283310delinsGTT	GRCh38
NC_000007.13:g.24322927_24322929delinsGTT , CM000669.1:g.24322927_24322929delinsGTT	GRCh37
NC_000007.12:g.24289452_24289454delinsGTT	NCBI36
NG_016148.1:g.4121_4123delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
XM_017012910.1:c.42-27611_42-27609delinsAAC	XP_016868399.1:n.42-27611_42-27609delinsAAC
XM_017012911.1:c.42-27611_42-27609delinsAAC	XP_016868400.1:n.42-27611_42-27609delinsAAC
XR_001745121.1:n.473+36047_473+36049delinsAAC
XR_001745122.1:n.345-86281_345-86279delinsAAC
XR_001745123.1:n.473+36047_473+36049delinsAAC
XR_001745124.1:n.473+36047_473+36049delinsAAC
XR_001745125.1:n.473+36047_473+36049delinsAAC
XR_001745126.1:n.473+36047_473+36049delinsAAC
XR_001745127.1:n.345-27611_345-27609delinsAAC
XR_001745129.1:n.473+36047_473+36049delinsAAC
XR_001745130.1:n.473+36047_473+36049delinsAAC
XR_001745131.1:n.473+36047_473+36049delinsAAC
XR_001745132.1:n.473+36047_473+36049delinsAAC