Canonical Allele Identifier: CA681651992

Gene: NAALAD2

Linked Data

• dbSNP Id: rs1263897703
• gnomAD v3: 11-90142380-A-C
• gnomAD v4: 11-90142380-A-C
• MyVariant Identifiers: chr11:g.89875548A>C (hg19) ; chr11:g.90142380A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.90142380A>C , CM000673.2:g.90142380A>C	GRCh38
NC_000011.9:g.89875548A>C , CM000673.1:g.89875548A>C	GRCh37
NC_000011.8:g.89515196A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000534061.6:c.195-4950A>C MANE Select	ENSP00000432481.1:n.195-4950A>C
ENST00000321955.8:c.195-4950A>C	ENSP00000320083.4:n.195-4950A>C
ENST00000375944.7:c.195-4950A>C	ENSP00000365111.3:n.195-4950A>C
ENST00000524501.1:n.255-4950A>C
ENST00000525171.5:c.195-4950A>C	ENSP00000435249.1:n.195-4950A>C
ENST00000525497.5:c.195-4950A>C	ENSP00000431989.1:n.195-4950A>C
ENST00000526637.1:c.33-4950A>C	ENSP00000435670.1:n.33-4950A>C
ENST00000527493.5:c.195-4950A>C	ENSP00000433710.1:n.195-4950A>C
ENST00000529090.5:n.290-4950A>C
ENST00000534061.5:c.195-4950A>C	ENSP00000432481.1:n.195-4950A>C
NM_001300930.1:c.195-4950A>C	NP_001287859.1:n.195-4950A>C
NM_005467.3:c.195-4950A>C	NP_005458.1:n.195-4950A>C
XM_005273701.2:c.33-4950A>C	XP_005273758.1:n.33-4950A>C
XM_011542550.1:c.195-4950A>C	XP_011540852.1:n.195-4950A>C
XM_011542551.1:c.195-4950A>C	XP_011540853.1:n.195-4950A>C
XM_011542552.1:c.300-4950A>C	XP_011540854.1:n.300-4950A>C
XM_011542553.1:c.195-4950A>C	XP_011540855.1:n.195-4950A>C
XM_011542554.1:c.195-4950A>C	XP_011540856.1:n.195-4950A>C
XM_017017043.2:c.300-4950A>C	XP_016872532.1:n.300-4950A>C
XM_017017044.2:c.300-4950A>C	XP_016872533.1:n.300-4950A>C
XM_017017045.1:c.33-4950A>C	XP_016872534.1:n.33-4950A>C
XM_017017046.2:c.300-4950A>C	XP_016872535.1:n.300-4950A>C
XR_001747707.2:n.476-4950A>C
XR_001747708.2:n.482-4950A>C
XR_001747709.2:n.473-4950A>C
XR_001747710.2:n.472-4950A>C
XR_001747711.2:n.472-4950A>C
NM_005467.4:c.195-4950A>C MANE Select	NP_005458.1:n.195-4950A>C
NM_001300930.2:c.195-4950A>C	NP_001287859.1:n.195-4950A>C