Canonical Allele Identifier: CA818424286

Gene: NKAIN2

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.124422361A>T , CM000668.2:g.124422361A>T	GRCh38
NC_000006.11:g.124743507A>T , CM000668.1:g.124743507A>T	GRCh37
NC_000006.10:g.124785206A>T	NCBI36
NG_021365.1:g.623439A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368417.6:c.273+67014A>T MANE Select	ENSP00000357402.1:n.273+67014A>T
ENST00000368416.5:c.273+67014A>T	ENSP00000357401.1:n.273+67014A>T
ENST00000368417.5:c.273+67014A>T	ENSP00000357402.1:n.273+67014A>T
ENST00000545433.2:c.270+67014A>T	ENSP00000437798.2:n.270+67014A>T
NM_001040214.2:c.273+67014A>T	NP_001035304.1:n.273+67014A>T
NM_001300737.1:c.270+67014A>T	NP_001287666.1:n.270+67014A>T
NM_001300738.1:c.-11-15542A>T	NP_001287667.1:n.-11-15542A>T
NM_001300740.1:c.-34+67014A>T	NP_001287669.1:n.-34+67014A>T
NM_153355.4:c.273+67014A>T	NP_699186.2:n.273+67014A>T
XM_005266834.2:c.273+67014A>T	XP_005266891.1:n.273+67014A>T
XM_011535501.1:c.273+67014A>T	XP_011533803.1:n.273+67014A>T
XM_011535502.1:c.270+67014A>T	XP_011533804.1:n.270+67014A>T
XM_011535503.1:c.192+139219A>T	XP_011533805.1:n.192+139219A>T
XM_011535501.3:c.273+67014A>T	XP_011533803.1:n.273+67014A>T
XM_011535503.3:c.192+139219A>T	XP_011533805.1:n.192+139219A>T
XM_017010318.2:c.192+139219A>T	XP_016865807.1:n.192+139219A>T
XM_017010319.2:c.273+67014A>T	XP_016865808.1:n.273+67014A>T
XM_024446340.1:c.270+67014A>T	XP_024302108.1:n.270+67014A>T
NM_001040214.3:c.273+67014A>T MANE Select	NP_001035304.1:n.273+67014A>T
NM_001300737.2:c.270+67014A>T	NP_001287666.1:n.270+67014A>T
NM_001300738.2:c.-11-15542A>T	NP_001287667.1:n.-11-15542A>T
NM_153355.5:c.273+67014A>T	NP_699186.2:n.273+67014A>T