Canonical Allele Identifier: CA1694873203

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24283374_24283376delinsTAA , CM000669.2:g.24283374_24283376delinsTAA	GRCh38
NC_000007.13:g.24322993_24322995delinsTAA , CM000669.1:g.24322993_24322995delinsTAA	GRCh37
NC_000007.12:g.24289518_24289520delinsTAA	NCBI36
NG_016148.1:g.4187_4189delinsTAA

Transcript Alleles

HGVS	Amino-acid Change
XM_017012910.1:c.42-27677_42-27675delinsTTA	XP_016868399.1:n.42-27677_42-27675delinsTTA
XM_017012911.1:c.42-27677_42-27675delinsTTA	XP_016868400.1:n.42-27677_42-27675delinsTTA
XR_001745121.1:n.473+35981_473+35983delinsTTA
XR_001745122.1:n.345-86347_345-86345delinsTTA
XR_001745123.1:n.473+35981_473+35983delinsTTA
XR_001745124.1:n.473+35981_473+35983delinsTTA
XR_001745125.1:n.473+35981_473+35983delinsTTA
XR_001745126.1:n.473+35981_473+35983delinsTTA
XR_001745127.1:n.345-27677_345-27675delinsTTA
XR_001745129.1:n.473+35981_473+35983delinsTTA
XR_001745130.1:n.473+35981_473+35983delinsTTA
XR_001745131.1:n.473+35981_473+35983delinsTTA
XR_001745132.1:n.473+35981_473+35983delinsTTA