Canonical Allele Identifier: CA1421856624

Gene: NAALADL2

Linked Data

• dbSNP Id: rs1762154144

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.175337877G>A , CM000665.2:g.175337877G>A	GRCh38
NC_000003.11:g.175055666G>A , CM000665.1:g.175055666G>A	GRCh37
NC_000003.10:g.176538360G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454872.6:c.1090+13552G>A MANE Select	ENSP00000404705.1:n.1090+13552G>A
ENST00000414826.1:c.120+81347G>A	ENSP00000396969.1:n.120+81347G>A
ENST00000454872.5:c.1090+13552G>A	ENSP00000404705.1:n.1090+13552G>A
ENST00000473253.5:n.1322+13552G>A
ENST00000489299.5:n.829+13552G>A
ENST00000614002.4:c.1054+13552G>A	ENSP00000479989.1:n.1054+13552G>A
NM_207015.2:c.1090+13552G>A	NP_996898.2:n.1090+13552G>A
XM_006713560.2:c.1039+13552G>A	XP_006713623.1:n.1039+13552G>A
XM_011512612.1:c.1120+13552G>A	XP_011510914.1:n.1120+13552G>A
XM_011512613.1:c.1069+13552G>A	XP_011510915.1:n.1069+13552G>A
XM_011512614.1:c.1039+13552G>A	XP_011510916.1:n.1039+13552G>A
XM_011512615.1:c.1120+13552G>A	XP_011510917.1:n.1120+13552G>A
XM_011512616.1:c.571+13552G>A	XP_011510918.1:n.571+13552G>A
XM_011512617.1:c.1120+13552G>A	XP_011510919.1:n.1120+13552G>A
XM_006713560.3:c.1039+13552G>A	XP_006713623.1:n.1039+13552G>A
XM_011512612.3:c.1120+13552G>A	XP_011510914.1:n.1120+13552G>A
XM_011512613.2:c.1069+13552G>A	XP_011510915.1:n.1069+13552G>A
XM_011512615.3:c.1120+13552G>A	XP_011510917.1:n.1120+13552G>A
XM_011512616.3:c.571+13552G>A	XP_011510918.1:n.571+13552G>A
XM_011512617.3:c.1120+13552G>A	XP_011510919.1:n.1120+13552G>A
XM_017006070.2:c.1039+13552G>A	XP_016861559.1:n.1039+13552G>A
XM_017006071.2:c.1039+13552G>A	XP_016861560.1:n.1039+13552G>A
XM_017006072.2:c.1039+13552G>A	XP_016861561.1:n.1039+13552G>A
XM_017006073.2:c.1039+13552G>A	XP_016861562.1:n.1039+13552G>A
XM_017006074.2:c.1039+13552G>A	XP_016861563.1:n.1039+13552G>A
XM_017006075.2:c.1039+13552G>A	XP_016861564.1:n.1039+13552G>A
XM_017006076.2:c.1039+13552G>A	XP_016861565.1:n.1039+13552G>A
XM_017006077.2:c.1039+13552G>A	XP_016861566.1:n.1039+13552G>A
XM_017006078.2:c.1039+13552G>A	XP_016861567.1:n.1039+13552G>A
XM_017006079.2:c.1039+13552G>A	XP_016861568.1:n.1039+13552G>A
XM_017006080.2:c.1039+13552G>A	XP_016861569.1:n.1039+13552G>A
XM_017006081.2:c.1120+13552G>A	XP_016861570.1:n.1120+13552G>A
XM_017006082.2:c.1039+13552G>A	XP_016861571.1:n.1039+13552G>A
XM_017006083.2:c.511+13552G>A	XP_016861572.1:n.511+13552G>A
NM_207015.3:c.1090+13552G>A MANE Select	NP_996898.2:n.1090+13552G>A