Canonical Allele Identifier: CA2124039558

Gene: GZMB

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24632763_24632765delinsCCT , CM000676.2:g.24632763_24632765delinsCCT	GRCh38
NC_000014.8:g.25101969_25101971delinsCCT , CM000676.1:g.25101969_25101971delinsCCT	GRCh37
NC_000014.7:g.24171809_24171811delinsCCT	NCBI36
NG_028340.1:g.6462_6464delinsAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216341.9:c.203+150_203+152delinsAGG MANE Select	ENSP00000216341.4:n.203+150_203+152delinsAGG
ENST00000216341.8:c.203+150_203+152delinsAGG	ENSP00000216341.4:n.203+150_203+152delinsAGG
ENST00000382540.5:c.204-46_204-44delinsAGG	ENSP00000371980.1:n.204-46_204-44delinsAGG
ENST00000382542.5:c.203+150_203+152delinsAGG	ENSP00000371982.2:n.203+150_203+152delinsAGG
ENST00000415355.7:c.167+150_167+152delinsAGG	ENSP00000387385.3:n.167+150_167+152delinsAGG
ENST00000526004.1:c.203+150_203+152delinsAGG	ENSP00000434213.1:n.203+150_203+152delinsAGG
ENST00000530830.1:c.*126+150_*126+152delinsAGG	ENSP00000435084.1:n.*126+150_*126+152delinsAGG
ENST00000532263.5:c.56-647_56-645delinsAGG	ENSP00000432074.1:n.56-647_56-645delinsAGG
ENST00000554242.5:c.203+150_203+152delinsAGG	ENSP00000450535.1:n.203+150_203+152delinsAGG
ENST00000616551.1:c.52-644_52-642delinsAGG	ENSP00000479643.1:n.52-644_52-642delinsAGG
NM_004131.4:c.203+150_203+152delinsAGG	NP_004122.2:n.203+150_203+152delinsAGG
XM_011536685.1:c.167+150_167+152delinsAGG	XP_011534987.1:n.167+150_167+152delinsAGG
NM_001346011.1:c.167+150_167+152delinsAGG	NP_001332940.1:n.167+150_167+152delinsAGG
NM_004131.5:c.203+150_203+152delinsAGG	NP_004122.2:n.203+150_203+152delinsAGG
NR_144343.1:n.312+150_312+152delinsAGG
NM_004131.6:c.203+150_203+152delinsAGG MANE Select	NP_004122.2:n.203+150_203+152delinsAGG
NM_001346011.2:c.167+150_167+152delinsAGG	NP_001332940.1:n.167+150_167+152delinsAGG
NR_144343.2:n.233+150_233+152delinsAGG