Canonical Allele Identifier: CA1421856632

Gene: NAALADL2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.175337889T= , CM000665.2:g.175337889T=	GRCh38
NC_000003.11:g.175055678T= , CM000665.1:g.175055678T=	GRCh37
NC_000003.10:g.176538372T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454872.6:c.1090+13564T= MANE Select	ENSP00000404705.1:n.1090+13564T=
ENST00000414826.1:c.120+81359T=	ENSP00000396969.1:n.120+81359T=
ENST00000454872.5:c.1090+13564T=	ENSP00000404705.1:n.1090+13564T=
ENST00000473253.5:n.1322+13564T=
ENST00000489299.5:n.829+13564T=
ENST00000614002.4:c.1054+13564T=	ENSP00000479989.1:n.1054+13564T=
NM_207015.2:c.1090+13564T=	NP_996898.2:n.1090+13564T=
XM_006713560.2:c.1039+13564T=	XP_006713623.1:n.1039+13564T=
XM_011512612.1:c.1120+13564T=	XP_011510914.1:n.1120+13564T=
XM_011512613.1:c.1069+13564T=	XP_011510915.1:n.1069+13564T=
XM_011512614.1:c.1039+13564T=	XP_011510916.1:n.1039+13564T=
XM_011512615.1:c.1120+13564T=	XP_011510917.1:n.1120+13564T=
XM_011512616.1:c.571+13564T=	XP_011510918.1:n.571+13564T=
XM_011512617.1:c.1120+13564T=	XP_011510919.1:n.1120+13564T=
XM_006713560.3:c.1039+13564T=	XP_006713623.1:n.1039+13564T=
XM_011512612.3:c.1120+13564T=	XP_011510914.1:n.1120+13564T=
XM_011512613.2:c.1069+13564T=	XP_011510915.1:n.1069+13564T=
XM_011512615.3:c.1120+13564T=	XP_011510917.1:n.1120+13564T=
XM_011512616.3:c.571+13564T=	XP_011510918.1:n.571+13564T=
XM_011512617.3:c.1120+13564T=	XP_011510919.1:n.1120+13564T=
XM_017006070.2:c.1039+13564T=	XP_016861559.1:n.1039+13564T=
XM_017006071.2:c.1039+13564T=	XP_016861560.1:n.1039+13564T=
XM_017006072.2:c.1039+13564T=	XP_016861561.1:n.1039+13564T=
XM_017006073.2:c.1039+13564T=	XP_016861562.1:n.1039+13564T=
XM_017006074.2:c.1039+13564T=	XP_016861563.1:n.1039+13564T=
XM_017006075.2:c.1039+13564T=	XP_016861564.1:n.1039+13564T=
XM_017006076.2:c.1039+13564T=	XP_016861565.1:n.1039+13564T=
XM_017006077.2:c.1039+13564T=	XP_016861566.1:n.1039+13564T=
XM_017006078.2:c.1039+13564T=	XP_016861567.1:n.1039+13564T=
XM_017006079.2:c.1039+13564T=	XP_016861568.1:n.1039+13564T=
XM_017006080.2:c.1039+13564T=	XP_016861569.1:n.1039+13564T=
XM_017006081.2:c.1120+13564T=	XP_016861570.1:n.1120+13564T=
XM_017006082.2:c.1039+13564T=	XP_016861571.1:n.1039+13564T=
XM_017006083.2:c.511+13564T=	XP_016861572.1:n.511+13564T=
NM_207015.3:c.1090+13564T= MANE Select	NP_996898.2:n.1090+13564T=