Canonical Allele Identifier: CA12207291

Gene: NKAIN2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.124629917A>C , CM000668.2:g.124629917A>C	GRCh38
NC_000006.11:g.124951063A>C , CM000668.1:g.124951063A>C	GRCh37
NC_000006.10:g.124992762A>C	NCBI36
NG_021365.1:g.830995A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368417.6:c.274-28269A>C MANE Select	ENSP00000357402.1:n.274-28269A>C
ENST00000368416.5:c.274-28269A>C	ENSP00000357401.1:n.274-28269A>C
ENST00000368417.5:c.274-28269A>C	ENSP00000357402.1:n.274-28269A>C
ENST00000545433.2:c.278-28276A>C	ENSP00000437798.2:n.278-28276A>C
NM_001040214.2:c.274-28269A>C	NP_001035304.1:n.274-28269A>C
NM_001300737.1:c.271-28269A>C	NP_001287666.1:n.271-28269A>C
NM_001300738.1:c.4-28269A>C	NP_001287667.1:n.4-28269A>C
NM_001300740.1:c.-33-28269A>C	NP_001287669.1:n.-33-28269A>C
NM_153355.4:c.274-161422A>C	NP_699186.2:n.274-161422A>C
XM_005266834.2:c.274-28269A>C	XP_005266891.1:n.274-28269A>C
XM_011535501.1:c.274-28269A>C	XP_011533803.1:n.274-28269A>C
XM_011535502.1:c.271-28269A>C	XP_011533804.1:n.271-28269A>C
XM_011535503.1:c.193-28269A>C	XP_011533805.1:n.193-28269A>C
XM_011535501.3:c.274-28269A>C	XP_011533803.1:n.274-28269A>C
XM_011535503.3:c.193-28269A>C	XP_011533805.1:n.193-28269A>C
XM_017010318.2:c.193-28269A>C	XP_016865807.1:n.193-28269A>C
XM_017010319.2:c.274-161422A>C	XP_016865808.1:n.274-161422A>C
XM_024446340.1:c.271-28269A>C	XP_024302108.1:n.271-28269A>C
NM_001040214.3:c.274-28269A>C MANE Select	NP_001035304.1:n.274-28269A>C
NM_001300737.2:c.271-28269A>C	NP_001287666.1:n.271-28269A>C
NM_001300738.2:c.4-28269A>C	NP_001287667.1:n.4-28269A>C
NM_153355.5:c.274-161422A>C	NP_699186.2:n.274-161422A>C