Canonical Allele Identifier: CA11387720
Gene: NAALADL2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1463525

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.175243598T>C , CM000665.2:g.175243598T>C GRCh38
NC_000003.11:g.174961387T>C , CM000665.1:g.174961387T>C GRCh37
NC_000003.10:g.176444081T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_207015.2:c.819+9394T>C VV NP_996898.2:p.=
NR_046713.1:n.41-1168A>G
XM_006713560.2:c.768+9394T>C XP_006713623.1:p.=
XM_011512612.1:c.849+9394T>C XP_011510914.1:p.=
XM_011512613.1:c.798+9394T>C XP_011510915.1:p.=
XM_011512614.1:c.768+9394T>C XP_011510916.1:p.=
XM_011512615.1:c.849+9394T>C XP_011510917.1:p.=
XM_011512616.1:c.300+9394T>C XP_011510918.1:p.=
XM_011512617.1:c.849+9394T>C XP_011510919.1:p.=
XM_006713560.3:c.768+9394T>C XP_006713623.1:p.=
XM_011512612.3:c.849+9394T>C XP_011510914.1:p.=
XM_011512613.2:c.798+9394T>C XP_011510915.1:p.=
XM_011512615.3:c.849+9394T>C XP_011510917.1:p.=
XM_011512616.3:c.300+9394T>C XP_011510918.1:p.=
XM_011512617.3:c.849+9394T>C XP_011510919.1:p.=
XM_017006070.2:c.768+9394T>C XP_016861559.1:p.=
XM_017006071.2:c.768+9394T>C XP_016861560.1:p.=
XM_017006072.2:c.768+9394T>C XP_016861561.1:p.=
XM_017006073.2:c.768+9394T>C XP_016861562.1:p.=
XM_017006074.2:c.768+9394T>C XP_016861563.1:p.=
XM_017006075.2:c.768+9394T>C XP_016861564.1:p.=
XM_017006076.2:c.768+9394T>C XP_016861565.1:p.=
XM_017006077.2:c.768+9394T>C XP_016861566.1:p.=
XM_017006078.2:c.768+9394T>C XP_016861567.1:p.=
XM_017006079.2:c.768+9394T>C XP_016861568.1:p.=
XM_017006080.2:c.768+9394T>C XP_016861569.1:p.=
XM_017006081.2:c.849+9394T>C XP_016861570.1:p.=
XM_017006082.2:c.768+9394T>C XP_016861571.1:p.=
XM_017006083.2:c.240+9394T>C XP_016861572.1:p.=
NM_207015.3:c.819+9394T>C VV MANE Preferred NP_996898.2:p.=
ENST00000454872.5:c.819+9394T>C ENSP00000404705.1:p.=
ENST00000473253.5:n.1051+9394T>C
ENST00000485853.5:n.905+9394T>C
ENST00000489299.5:n.558+9394T>C
ENST00000614002.4:n.783+9394T>C ENSP00000479989.1:p.=