Canonical Allele Identifier: CA12377093

Gene: NKAIN2

Linked Data

• dbSNP Id: rs9491140
• gnomAD v2: 6-124691237-C-T
• gnomAD v3: 6-124370091-C-T
• gnomAD v4: 6-124370091-C-T
• MyVariant Identifiers: chr6:g.124691237C>T (hg19) ; chr6:g.124370091C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.124370091C>T , CM000668.2:g.124370091C>T	GRCh38
NC_000006.11:g.124691237C>T , CM000668.1:g.124691237C>T	GRCh37
NC_000006.10:g.124732936C>T	NCBI36
NG_021365.1:g.571169C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368417.6:c.273+14744C>T MANE Select	ENSP00000357402.1:n.273+14744C>T
ENST00000368416.5:c.273+14744C>T	ENSP00000357401.1:n.273+14744C>T
ENST00000368417.5:c.273+14744C>T	ENSP00000357402.1:n.273+14744C>T
ENST00000476571.1:n.397+14744C>T
ENST00000545433.2:c.270+14744C>T	ENSP00000437798.2:n.270+14744C>T
NM_001040214.2:c.273+14744C>T	NP_001035304.1:n.273+14744C>T
NM_001300737.1:c.270+14744C>T	NP_001287666.1:n.270+14744C>T
NM_001300738.1:c.-12+14744C>T	NP_001287667.1:n.-12+14744C>T
NM_001300740.1:c.-34+14744C>T	NP_001287669.1:n.-34+14744C>T
NM_153355.4:c.273+14744C>T	NP_699186.2:n.273+14744C>T
XM_005266834.2:c.273+14744C>T	XP_005266891.1:n.273+14744C>T
XM_011535501.1:c.273+14744C>T	XP_011533803.1:n.273+14744C>T
XM_011535502.1:c.270+14744C>T	XP_011533804.1:n.270+14744C>T
XM_011535503.1:c.192+86949C>T	XP_011533805.1:n.192+86949C>T
XM_011535501.3:c.273+14744C>T	XP_011533803.1:n.273+14744C>T
XM_011535503.3:c.192+86949C>T	XP_011533805.1:n.192+86949C>T
XM_017010318.2:c.192+86949C>T	XP_016865807.1:n.192+86949C>T
XM_017010319.2:c.273+14744C>T	XP_016865808.1:n.273+14744C>T
XM_024446340.1:c.270+14744C>T	XP_024302108.1:n.270+14744C>T
NM_001040214.3:c.273+14744C>T MANE Select	NP_001035304.1:n.273+14744C>T
NM_001300737.2:c.270+14744C>T	NP_001287666.1:n.270+14744C>T
NM_001300738.2:c.-12+14744C>T	NP_001287667.1:n.-12+14744C>T
NM_153355.5:c.273+14744C>T	NP_699186.2:n.273+14744C>T