Canonical Allele Identifier: CA2542144897

Gene: NAALADL2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.175337995_175337997del , CM000665.2:g.175337995_175337997del	GRCh38
NC_000003.11:g.175055784_175055786del , CM000665.1:g.175055784_175055786del	GRCh37
NC_000003.10:g.176538478_176538480del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000454872.6:c.1090+13670_1090+13672del MANE Select	ENSP00000404705.1:n.1090+13670_1090+13672del
ENST00000414826.1:c.120+81465_120+81467del	ENSP00000396969.1:n.120+81465_120+81467del
ENST00000454872.5:c.1090+13670_1090+13672del	ENSP00000404705.1:n.1090+13670_1090+13672del
ENST00000473253.5:n.1322+13670_1322+13672del
ENST00000489299.5:n.829+13670_829+13672del
ENST00000614002.4:c.1054+13670_1054+13672del	ENSP00000479989.1:n.1054+13670_1054+13672del
NM_207015.2:c.1090+13670_1090+13672del	NP_996898.2:n.1090+13670_1090+13672del
XM_006713560.2:c.1039+13670_1039+13672del	XP_006713623.1:n.1039+13670_1039+13672del
XM_011512612.1:c.1120+13670_1120+13672del	XP_011510914.1:n.1120+13670_1120+13672del
XM_011512613.1:c.1069+13670_1069+13672del	XP_011510915.1:n.1069+13670_1069+13672del
XM_011512614.1:c.1039+13670_1039+13672del	XP_011510916.1:n.1039+13670_1039+13672del
XM_011512615.1:c.1120+13670_1120+13672del	XP_011510917.1:n.1120+13670_1120+13672del
XM_011512616.1:c.571+13670_571+13672del	XP_011510918.1:n.571+13670_571+13672del
XM_011512617.1:c.1120+13670_1120+13672del	XP_011510919.1:n.1120+13670_1120+13672del
XM_006713560.3:c.1039+13670_1039+13672del	XP_006713623.1:n.1039+13670_1039+13672del
XM_011512612.3:c.1120+13670_1120+13672del	XP_011510914.1:n.1120+13670_1120+13672del
XM_011512613.2:c.1069+13670_1069+13672del	XP_011510915.1:n.1069+13670_1069+13672del
XM_011512615.3:c.1120+13670_1120+13672del	XP_011510917.1:n.1120+13670_1120+13672del
XM_011512616.3:c.571+13670_571+13672del	XP_011510918.1:n.571+13670_571+13672del
XM_011512617.3:c.1120+13670_1120+13672del	XP_011510919.1:n.1120+13670_1120+13672del
XM_017006070.2:c.1039+13670_1039+13672del	XP_016861559.1:n.1039+13670_1039+13672del
XM_017006071.2:c.1039+13670_1039+13672del	XP_016861560.1:n.1039+13670_1039+13672del
XM_017006072.2:c.1039+13670_1039+13672del	XP_016861561.1:n.1039+13670_1039+13672del
XM_017006073.2:c.1039+13670_1039+13672del	XP_016861562.1:n.1039+13670_1039+13672del
XM_017006074.2:c.1039+13670_1039+13672del	XP_016861563.1:n.1039+13670_1039+13672del
XM_017006075.2:c.1039+13670_1039+13672del	XP_016861564.1:n.1039+13670_1039+13672del
XM_017006076.2:c.1039+13670_1039+13672del	XP_016861565.1:n.1039+13670_1039+13672del
XM_017006077.2:c.1039+13670_1039+13672del	XP_016861566.1:n.1039+13670_1039+13672del
XM_017006078.2:c.1039+13670_1039+13672del	XP_016861567.1:n.1039+13670_1039+13672del
XM_017006079.2:c.1039+13670_1039+13672del	XP_016861568.1:n.1039+13670_1039+13672del
XM_017006080.2:c.1039+13670_1039+13672del	XP_016861569.1:n.1039+13670_1039+13672del
XM_017006081.2:c.1120+13670_1120+13672del	XP_016861570.1:n.1120+13670_1120+13672del
XM_017006082.2:c.1039+13670_1039+13672del	XP_016861571.1:n.1039+13670_1039+13672del
XM_017006083.2:c.511+13670_511+13672del	XP_016861572.1:n.511+13670_511+13672del
NM_207015.3:c.1090+13670_1090+13672del MANE Select	NP_996898.2:n.1090+13670_1090+13672del