Canonical Allele Identifier: CA2800907467

Gene: GZMB

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24632771_24632772insCAAC , CM000676.2:g.24632771_24632772insCAAC	GRCh38
NC_000014.8:g.25101977_25101978insCAAC , CM000676.1:g.25101977_25101978insCAAC	GRCh37
NC_000014.7:g.24171817_24171818insCAAC	NCBI36
NG_028340.1:g.6456_6457insTTGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000216341.9:c.203+144_203+145insTTGG MANE Select	ENSP00000216341.4:n.203+144_203+145insTTGG
ENST00000216341.8:c.203+144_203+145insTTGG	ENSP00000216341.4:n.203+144_203+145insTTGG
ENST00000382540.5:c.204-52_204-51insTTGG	ENSP00000371980.1:n.204-52_204-51insTTGG
ENST00000382542.5:c.203+144_203+145insTTGG	ENSP00000371982.2:n.203+144_203+145insTTGG
ENST00000415355.7:c.167+144_167+145insTTGG	ENSP00000387385.3:n.167+144_167+145insTTGG
ENST00000526004.1:c.203+144_203+145insTTGG	ENSP00000434213.1:n.203+144_203+145insTTGG
ENST00000530830.1:c.*126+144_*126+145insTTGG	ENSP00000435084.1:n.*126+144_*126+145insTTGG
ENST00000532263.5:c.56-653_56-652insTTGG	ENSP00000432074.1:n.56-653_56-652insTTGG
ENST00000554242.5:c.203+144_203+145insTTGG	ENSP00000450535.1:n.203+144_203+145insTTGG
ENST00000616551.1:c.52-650_52-649insTTGG	ENSP00000479643.1:n.52-650_52-649insTTGG
NM_004131.4:c.203+144_203+145insTTGG	NP_004122.2:n.203+144_203+145insTTGG
XM_011536685.1:c.167+144_167+145insTTGG	XP_011534987.1:n.167+144_167+145insTTGG
NM_001346011.1:c.167+144_167+145insTTGG	NP_001332940.1:n.167+144_167+145insTTGG
NM_004131.5:c.203+144_203+145insTTGG	NP_004122.2:n.203+144_203+145insTTGG
NR_144343.1:n.312+144_312+145insTTGG
NM_004131.6:c.203+144_203+145insTTGG MANE Select	NP_004122.2:n.203+144_203+145insTTGG
NM_001346011.2:c.167+144_167+145insTTGG	NP_001332940.1:n.167+144_167+145insTTGG
NR_144343.2:n.233+144_233+145insTTGG