Canonical Allele Identifier: CA570355880

Gene: NKAIN2

Linked Data

• dbSNP Id: rs369059002
• gnomAD v2: 6-124302483-G-GA
• gnomAD v3: 6-123981338-G-GA
• gnomAD v4: 6-123981338-G-GA
• MyVariant Identifiers: chr6:g.124302484_124302485insA (hg19) ; chr6:g.124302483_124302484insA (hg19) ; chr6:g.123981339_123981340insA (hg38) ; chr6:g.123981338_123981339insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.123981347dup , CM000668.2:g.123981347dup	GRCh38
NC_000006.11:g.124302492dup , CM000668.1:g.124302492dup	GRCh37
NC_000006.10:g.124344191dup	NCBI36
NG_021365.1:g.182424dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368417.6:c.54+177093dup MANE Select	ENSP00000357402.1:n.54+177093dup
ENST00000368416.5:c.54+177093dup	ENSP00000357401.1:n.54+177093dup
ENST00000368417.5:c.54+177093dup	ENSP00000357402.1:n.54+177093dup
ENST00000476571.1:n.115-140531dup
NM_001040214.2:c.54+177093dup	NP_001035304.1:n.54+177093dup
NM_001300737.1:c.-13-140531dup	NP_001287666.1:n.-13-140531dup
NM_001300738.1:c.-231+177093dup	NP_001287667.1:n.-231+177093dup
NM_001300740.1:c.-253+176916dup	NP_001287669.1:n.-253+176916dup
NM_153355.4:c.54+177093dup	NP_699186.2:n.54+177093dup
XM_005266834.2:c.54+177093dup	XP_005266891.1:n.54+177093dup
XM_011535501.1:c.54+177093dup	XP_011533803.1:n.54+177093dup
XM_011535503.1:c.54+177093dup	XP_011533805.1:n.54+177093dup
XM_011535501.3:c.54+177093dup	XP_011533803.1:n.54+177093dup
XM_011535503.3:c.54+177093dup	XP_011533805.1:n.54+177093dup
XM_017010318.2:c.54+177093dup	XP_016865807.1:n.54+177093dup
XM_017010319.2:c.54+177093dup	XP_016865808.1:n.54+177093dup
XM_024446340.1:c.-13-140531dup	XP_024302108.1:n.-13-140531dup
NM_001040214.3:c.54+177093dup MANE Select	NP_001035304.1:n.54+177093dup
NM_001300737.2:c.-13-140531dup	NP_001287666.1:n.-13-140531dup
NM_001300738.2:c.-231+177093dup	NP_001287667.1:n.-231+177093dup
NM_153355.5:c.54+177093dup	NP_699186.2:n.54+177093dup