Canonical Allele Identifier: CA2124039639

Gene: GZMB

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24632908_24632909delinsTC , CM000676.2:g.24632908_24632909delinsTC	GRCh38
NC_000014.8:g.25102114_25102115delinsTC , CM000676.1:g.25102114_25102115delinsTC	GRCh37
NC_000014.7:g.24171954_24171955delinsTC	NCBI36
NG_028340.1:g.6318_6319delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216341.9:c.203+6_203+7delinsGA MANE Select	ENSP00000216341.4:n.203+6_203+7delinsGA
ENST00000216341.8:c.203+6_203+7delinsGA	ENSP00000216341.4:n.203+6_203+7delinsGA
ENST00000382540.5:c.203+6_203+7delinsGA	ENSP00000371980.1:n.203+6_203+7delinsGA
ENST00000382542.5:c.203+6_203+7delinsGA	ENSP00000371982.2:n.203+6_203+7delinsGA
ENST00000415355.7:c.167+6_167+7delinsGA	ENSP00000387385.3:n.167+6_167+7delinsGA
ENST00000526004.1:c.203+6_203+7delinsGA	ENSP00000434213.1:n.203+6_203+7delinsGA
ENST00000530830.1:c.*126+6_*126+7delinsGA	ENSP00000435084.1:n.*126+6_*126+7delinsGA
ENST00000532263.5:c.56-791_56-790delinsGA	ENSP00000432074.1:n.56-791_56-790delinsGA
ENST00000554242.5:c.203+6_203+7delinsGA	ENSP00000450535.1:n.203+6_203+7delinsGA
ENST00000616551.1:c.52-788_52-787delinsGA	ENSP00000479643.1:n.52-788_52-787delinsGA
NM_004131.4:c.203+6_203+7delinsGA	NP_004122.2:n.203+6_203+7delinsGA
XM_011536685.1:c.167+6_167+7delinsGA	XP_011534987.1:n.167+6_167+7delinsGA
NM_001346011.1:c.167+6_167+7delinsGA	NP_001332940.1:n.167+6_167+7delinsGA
NM_004131.5:c.203+6_203+7delinsGA	NP_004122.2:n.203+6_203+7delinsGA
NR_144343.1:n.312+6_312+7delinsGA
NM_004131.6:c.203+6_203+7delinsGA MANE Select	NP_004122.2:n.203+6_203+7delinsGA
NM_001346011.2:c.167+6_167+7delinsGA	NP_001332940.1:n.167+6_167+7delinsGA
NR_144343.2:n.233+6_233+7delinsGA