Canonical Allele Identifier: CA648422712

Gene: NAALADL2

Linked Data

• COSMIC: COSN7836570

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.175346946A>G , CM000665.2:g.175346946A>G	GRCh38
NC_000003.11:g.175064735A>G , CM000665.1:g.175064735A>G	GRCh37
NC_000003.10:g.176547429A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000454872.6:c.1090+22621A>G MANE Select	ENSP00000404705.1:n.1090+22621A>G
ENST00000414826.1:c.120+90416A>G	ENSP00000396969.1:n.120+90416A>G
ENST00000454872.5:c.1090+22621A>G	ENSP00000404705.1:n.1090+22621A>G
ENST00000473253.5:n.1322+22621A>G
ENST00000489299.5:n.829+22621A>G
ENST00000614002.4:c.1054+22621A>G	ENSP00000479989.1:n.1054+22621A>G
NM_207015.2:c.1090+22621A>G	NP_996898.2:n.1090+22621A>G
XM_006713560.2:c.1039+22621A>G	XP_006713623.1:n.1039+22621A>G
XM_011512612.1:c.1120+22621A>G	XP_011510914.1:n.1120+22621A>G
XM_011512613.1:c.1069+22621A>G	XP_011510915.1:n.1069+22621A>G
XM_011512614.1:c.1039+22621A>G	XP_011510916.1:n.1039+22621A>G
XM_011512615.1:c.1120+22621A>G	XP_011510917.1:n.1120+22621A>G
XM_011512616.1:c.571+22621A>G	XP_011510918.1:n.571+22621A>G
XM_011512617.1:c.1120+22621A>G	XP_011510919.1:n.1120+22621A>G
XM_006713560.3:c.1039+22621A>G	XP_006713623.1:n.1039+22621A>G
XM_011512612.3:c.1120+22621A>G	XP_011510914.1:n.1120+22621A>G
XM_011512613.2:c.1069+22621A>G	XP_011510915.1:n.1069+22621A>G
XM_011512615.3:c.1120+22621A>G	XP_011510917.1:n.1120+22621A>G
XM_011512616.3:c.571+22621A>G	XP_011510918.1:n.571+22621A>G
XM_011512617.3:c.1120+22621A>G	XP_011510919.1:n.1120+22621A>G
XM_017006070.2:c.1039+22621A>G	XP_016861559.1:n.1039+22621A>G
XM_017006071.2:c.1039+22621A>G	XP_016861560.1:n.1039+22621A>G
XM_017006072.2:c.1039+22621A>G	XP_016861561.1:n.1039+22621A>G
XM_017006073.2:c.1039+22621A>G	XP_016861562.1:n.1039+22621A>G
XM_017006074.2:c.1039+22621A>G	XP_016861563.1:n.1039+22621A>G
XM_017006075.2:c.1039+22621A>G	XP_016861564.1:n.1039+22621A>G
XM_017006076.2:c.1039+22621A>G	XP_016861565.1:n.1039+22621A>G
XM_017006077.2:c.1039+22621A>G	XP_016861566.1:n.1039+22621A>G
XM_017006078.2:c.1039+22621A>G	XP_016861567.1:n.1039+22621A>G
XM_017006079.2:c.1039+22621A>G	XP_016861568.1:n.1039+22621A>G
XM_017006080.2:c.1039+22621A>G	XP_016861569.1:n.1039+22621A>G
XM_017006081.2:c.1120+22621A>G	XP_016861570.1:n.1120+22621A>G
XM_017006082.2:c.1039+22621A>G	XP_016861571.1:n.1039+22621A>G
XM_017006083.2:c.511+22621A>G	XP_016861572.1:n.511+22621A>G
NM_207015.3:c.1090+22621A>G MANE Select	NP_996898.2:n.1090+22621A>G