Canonical Allele Identifier: CA1660804116

Gene: NKAIN2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.124238607G= , CM000668.2:g.124238607G=	GRCh38
NC_000006.11:g.124559753G= , CM000668.1:g.124559753G=	GRCh37
NC_000006.10:g.124601452G=	NCBI36
NG_021365.1:g.439685G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000368417.6:c.55-44398G= MANE Select	ENSP00000357402.1:n.55-44398G=
ENST00000368416.5:c.55-44398G=	ENSP00000357401.1:n.55-44398G=
ENST00000368417.5:c.55-44398G=	ENSP00000357402.1:n.55-44398G=
ENST00000476571.1:n.179-44398G=
ENST00000545433.2:c.52-44398G=	ENSP00000437798.2:n.52-44398G=
NM_001040214.2:c.55-44398G=	NP_001035304.1:n.55-44398G=
NM_001300737.1:c.52-44398G=	NP_001287666.1:n.52-44398G=
NM_001300738.1:c.-230-44398G=	NP_001287667.1:n.-230-44398G=
NM_001300740.1:c.-252-44398G=	NP_001287669.1:n.-252-44398G=
NM_153355.4:c.55-44398G=	NP_699186.2:n.55-44398G=
XM_005266834.2:c.55-44398G=	XP_005266891.1:n.55-44398G=
XM_011535501.1:c.55-44398G=	XP_011533803.1:n.55-44398G=
XM_011535502.1:c.52-44398G=	XP_011533804.1:n.52-44398G=
XM_011535503.1:c.55-44398G=	XP_011533805.1:n.55-44398G=
XM_011535501.3:c.55-44398G=	XP_011533803.1:n.55-44398G=
XM_011535503.3:c.55-44398G=	XP_011533805.1:n.55-44398G=
XM_017010318.2:c.55-44398G=	XP_016865807.1:n.55-44398G=
XM_017010319.2:c.55-44398G=	XP_016865808.1:n.55-44398G=
XM_024446340.1:c.52-44398G=	XP_024302108.1:n.52-44398G=
NM_001040214.3:c.55-44398G= MANE Select	NP_001035304.1:n.55-44398G=
NM_001300737.2:c.52-44398G=	NP_001287666.1:n.52-44398G=
NM_001300738.2:c.-230-44398G=	NP_001287667.1:n.-230-44398G=
NM_153355.5:c.55-44398G=	NP_699186.2:n.55-44398G=