Canonical Allele Identifier: CA1421856682

Gene: NAALADL2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.175337972_175337973delinsGA , CM000665.2:g.175337972_175337973delinsGA	GRCh38
NC_000003.11:g.175055761_175055762delinsGA , CM000665.1:g.175055761_175055762delinsGA	GRCh37
NC_000003.10:g.176538455_176538456delinsGA	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000454872.6:c.1090+13647_1090+13648delinsGA MANE Select	ENSP00000404705.1:n.1090+13647_1090+13648delinsGA
ENST00000414826.1:c.120+81442_120+81443delinsGA	ENSP00000396969.1:n.120+81442_120+81443delinsGA
ENST00000454872.5:c.1090+13647_1090+13648delinsGA	ENSP00000404705.1:n.1090+13647_1090+13648delinsGA
ENST00000473253.5:n.1322+13647_1322+13648delinsGA
ENST00000489299.5:n.829+13647_829+13648delinsGA
ENST00000614002.4:c.1054+13647_1054+13648delinsGA	ENSP00000479989.1:n.1054+13647_1054+13648delinsGA
NM_207015.2:c.1090+13647_1090+13648delinsGA	NP_996898.2:n.1090+13647_1090+13648delinsGA
XM_006713560.2:c.1039+13647_1039+13648delinsGA	XP_006713623.1:n.1039+13647_1039+13648delinsGA
XM_011512612.1:c.1120+13647_1120+13648delinsGA	XP_011510914.1:n.1120+13647_1120+13648delinsGA
XM_011512613.1:c.1069+13647_1069+13648delinsGA	XP_011510915.1:n.1069+13647_1069+13648delinsGA
XM_011512614.1:c.1039+13647_1039+13648delinsGA	XP_011510916.1:n.1039+13647_1039+13648delinsGA
XM_011512615.1:c.1120+13647_1120+13648delinsGA	XP_011510917.1:n.1120+13647_1120+13648delinsGA
XM_011512616.1:c.571+13647_571+13648delinsGA	XP_011510918.1:n.571+13647_571+13648delinsGA
XM_011512617.1:c.1120+13647_1120+13648delinsGA	XP_011510919.1:n.1120+13647_1120+13648delinsGA
XM_006713560.3:c.1039+13647_1039+13648delinsGA	XP_006713623.1:n.1039+13647_1039+13648delinsGA
XM_011512612.3:c.1120+13647_1120+13648delinsGA	XP_011510914.1:n.1120+13647_1120+13648delinsGA
XM_011512613.2:c.1069+13647_1069+13648delinsGA	XP_011510915.1:n.1069+13647_1069+13648delinsGA
XM_011512615.3:c.1120+13647_1120+13648delinsGA	XP_011510917.1:n.1120+13647_1120+13648delinsGA
XM_011512616.3:c.571+13647_571+13648delinsGA	XP_011510918.1:n.571+13647_571+13648delinsGA
XM_011512617.3:c.1120+13647_1120+13648delinsGA	XP_011510919.1:n.1120+13647_1120+13648delinsGA
XM_017006070.2:c.1039+13647_1039+13648delinsGA	XP_016861559.1:n.1039+13647_1039+13648delinsGA
XM_017006071.2:c.1039+13647_1039+13648delinsGA	XP_016861560.1:n.1039+13647_1039+13648delinsGA
XM_017006072.2:c.1039+13647_1039+13648delinsGA	XP_016861561.1:n.1039+13647_1039+13648delinsGA
XM_017006073.2:c.1039+13647_1039+13648delinsGA	XP_016861562.1:n.1039+13647_1039+13648delinsGA
XM_017006074.2:c.1039+13647_1039+13648delinsGA	XP_016861563.1:n.1039+13647_1039+13648delinsGA
XM_017006075.2:c.1039+13647_1039+13648delinsGA	XP_016861564.1:n.1039+13647_1039+13648delinsGA
XM_017006076.2:c.1039+13647_1039+13648delinsGA	XP_016861565.1:n.1039+13647_1039+13648delinsGA
XM_017006077.2:c.1039+13647_1039+13648delinsGA	XP_016861566.1:n.1039+13647_1039+13648delinsGA
XM_017006078.2:c.1039+13647_1039+13648delinsGA	XP_016861567.1:n.1039+13647_1039+13648delinsGA
XM_017006079.2:c.1039+13647_1039+13648delinsGA	XP_016861568.1:n.1039+13647_1039+13648delinsGA
XM_017006080.2:c.1039+13647_1039+13648delinsGA	XP_016861569.1:n.1039+13647_1039+13648delinsGA
XM_017006081.2:c.1120+13647_1120+13648delinsGA	XP_016861570.1:n.1120+13647_1120+13648delinsGA
XM_017006082.2:c.1039+13647_1039+13648delinsGA	XP_016861571.1:n.1039+13647_1039+13648delinsGA
XM_017006083.2:c.511+13647_511+13648delinsGA	XP_016861572.1:n.511+13647_511+13648delinsGA
NM_207015.3:c.1090+13647_1090+13648delinsGA MANE Select	NP_996898.2:n.1090+13647_1090+13648delinsGA