Canonical Allele Identifier: CA681651878

Gene: NAALAD2

Linked Data

• dbSNP Id: rs1223751832
• MyVariant Identifiers: chr11:g.89875348_89875349insAA (hg19) ; chr11:g.90142180_90142181insAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.90142181_90142182insAA , CM000673.2:g.90142181_90142182insAA	GRCh38
NC_000011.9:g.89875349_89875350insAA , CM000673.1:g.89875349_89875350insAA	GRCh37
NC_000011.8:g.89514997_89514998insAA	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000534061.6:c.195-5149_195-5148insAA MANE Select	ENSP00000432481.1:n.195-5149_195-5148insA...
ENST00000321955.8:c.195-5149_195-5148insAA	ENSP00000320083.4:n.195-5149_195-5148insA...
ENST00000375944.7:c.195-5149_195-5148insAA	ENSP00000365111.3:n.195-5149_195-5148insA...
ENST00000524501.1:n.255-5149_255-5148insAA
ENST00000525171.5:c.195-5149_195-5148insAA	ENSP00000435249.1:n.195-5149_195-5148insA...
ENST00000525497.5:c.195-5149_195-5148insAA	ENSP00000431989.1:n.195-5149_195-5148insA...
ENST00000526637.1:c.33-5149_33-5148insAA	ENSP00000435670.1:n.33-5149_33-5148insAA
ENST00000527493.5:c.195-5149_195-5148insAA	ENSP00000433710.1:n.195-5149_195-5148insA...
ENST00000529090.5:n.290-5149_290-5148insAA
ENST00000534061.5:c.195-5149_195-5148insAA	ENSP00000432481.1:n.195-5149_195-5148insA...
NM_001300930.1:c.195-5149_195-5148insAA	NP_001287859.1:n.195-5149_195-5148insAA
NM_005467.3:c.195-5149_195-5148insAA	NP_005458.1:n.195-5149_195-5148insAA
XM_005273701.2:c.33-5149_33-5148insAA	XP_005273758.1:n.33-5149_33-5148insAA
XM_011542550.1:c.195-5149_195-5148insAA	XP_011540852.1:n.195-5149_195-5148insAA
XM_011542551.1:c.195-5149_195-5148insAA	XP_011540853.1:n.195-5149_195-5148insAA
XM_011542552.1:c.300-5149_300-5148insAA	XP_011540854.1:n.300-5149_300-5148insAA
XM_011542553.1:c.195-5149_195-5148insAA	XP_011540855.1:n.195-5149_195-5148insAA
XM_011542554.1:c.195-5149_195-5148insAA	XP_011540856.1:n.195-5149_195-5148insAA
XM_017017043.2:c.300-5149_300-5148insAA	XP_016872532.1:n.300-5149_300-5148insAA
XM_017017044.2:c.300-5149_300-5148insAA	XP_016872533.1:n.300-5149_300-5148insAA
XM_017017045.1:c.33-5149_33-5148insAA	XP_016872534.1:n.33-5149_33-5148insAA
XM_017017046.2:c.300-5149_300-5148insAA	XP_016872535.1:n.300-5149_300-5148insAA
XR_001747707.2:n.476-5149_476-5148insAA
XR_001747708.2:n.482-5149_482-5148insAA
XR_001747709.2:n.473-5149_473-5148insAA
XR_001747710.2:n.472-5149_472-5148insAA
XR_001747711.2:n.472-5149_472-5148insAA
NM_005467.4:c.195-5149_195-5148insAA MANE Select	NP_005458.1:n.195-5149_195-5148insAA
NM_001300930.2:c.195-5149_195-5148insAA	NP_001287859.1:n.195-5149_195-5148insAA