Canonical Allele Identifier: CA917964997

Gene:

Linked Data

• dbSNP Id: rs1554349736

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24283308_24283312delinsTGC , CM000669.2:g.24283308_24283312delinsTGC	GRCh38
NC_000007.13:g.24322927_24322931delinsTGC , CM000669.1:g.24322927_24322931delinsTGC	GRCh37
NC_000007.12:g.24289452_24289456delinsTGC	NCBI36
NG_016148.1:g.4121_4125delinsTGC

Transcript Alleles

HGVS	Amino-acid Change
XM_017012910.1:c.42-27613_42-27609delinsGCA	XP_016868399.1:n.42-27613_42-27609delinsGCA
XM_017012911.1:c.42-27613_42-27609delinsGCA	XP_016868400.1:n.42-27613_42-27609delinsGCA
XR_001745121.1:n.473+36045_473+36049delinsGCA
XR_001745122.1:n.345-86283_345-86279delinsGCA
XR_001745123.1:n.473+36045_473+36049delinsGCA
XR_001745124.1:n.473+36045_473+36049delinsGCA
XR_001745125.1:n.473+36045_473+36049delinsGCA
XR_001745126.1:n.473+36045_473+36049delinsGCA
XR_001745127.1:n.345-27613_345-27609delinsGCA
XR_001745129.1:n.473+36045_473+36049delinsGCA
XR_001745130.1:n.473+36045_473+36049delinsGCA
XR_001745131.1:n.473+36045_473+36049delinsGCA
XR_001745132.1:n.473+36045_473+36049delinsGCA