Canonical Allele Identifier: CA226369131

Gene: NAALAD2

Linked Data

• dbSNP Id: rs914935637
• MyVariant Identifiers: chr11:g.89875378C>T (hg19) ; chr11:g.90142210C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.90142210C>T , CM000673.2:g.90142210C>T	GRCh38
NC_000011.9:g.89875378C>T , CM000673.1:g.89875378C>T	GRCh37
NC_000011.8:g.89515026C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000534061.6:c.195-5120C>T MANE Select	ENSP00000432481.1:n.195-5120C>T
ENST00000321955.8:c.195-5120C>T	ENSP00000320083.4:n.195-5120C>T
ENST00000375944.7:c.195-5120C>T	ENSP00000365111.3:n.195-5120C>T
ENST00000524501.1:n.255-5120C>T
ENST00000525171.5:c.195-5120C>T	ENSP00000435249.1:n.195-5120C>T
ENST00000525497.5:c.195-5120C>T	ENSP00000431989.1:n.195-5120C>T
ENST00000526637.1:c.33-5120C>T	ENSP00000435670.1:n.33-5120C>T
ENST00000527493.5:c.195-5120C>T	ENSP00000433710.1:n.195-5120C>T
ENST00000529090.5:n.290-5120C>T
ENST00000534061.5:c.195-5120C>T	ENSP00000432481.1:n.195-5120C>T
NM_001300930.1:c.195-5120C>T	NP_001287859.1:n.195-5120C>T
NM_005467.3:c.195-5120C>T	NP_005458.1:n.195-5120C>T
XM_005273701.2:c.33-5120C>T	XP_005273758.1:n.33-5120C>T
XM_011542550.1:c.195-5120C>T	XP_011540852.1:n.195-5120C>T
XM_011542551.1:c.195-5120C>T	XP_011540853.1:n.195-5120C>T
XM_011542552.1:c.300-5120C>T	XP_011540854.1:n.300-5120C>T
XM_011542553.1:c.195-5120C>T	XP_011540855.1:n.195-5120C>T
XM_011542554.1:c.195-5120C>T	XP_011540856.1:n.195-5120C>T
XM_017017043.2:c.300-5120C>T	XP_016872532.1:n.300-5120C>T
XM_017017044.2:c.300-5120C>T	XP_016872533.1:n.300-5120C>T
XM_017017045.1:c.33-5120C>T	XP_016872534.1:n.33-5120C>T
XM_017017046.2:c.300-5120C>T	XP_016872535.1:n.300-5120C>T
XR_001747707.2:n.476-5120C>T
XR_001747708.2:n.482-5120C>T
XR_001747709.2:n.473-5120C>T
XR_001747710.2:n.472-5120C>T
XR_001747711.2:n.472-5120C>T
NM_005467.4:c.195-5120C>T MANE Select	NP_005458.1:n.195-5120C>T
NM_001300930.2:c.195-5120C>T	NP_001287859.1:n.195-5120C>T