Canonical Allele Identifier: CA3295313

Gene: NAIP

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.71012816A>G , CM000667.2:g.71012816A>G	GRCh38
NC_000005.9:g.70308643A>G , CM000667.1:g.70308643A>G	GRCh37
NC_000005.8:g.70344399A>G	NCBI36
NG_008724.1:g.17299T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517649.6:c.100T>C MANE Select	ENSP00000428657.2:p.Leu34=
ENST00000194097.8:c.100T>C	ENSP00000443944.1:p.Leu34=
ENST00000503719.6:c.182+7843T>C	ENSP00000424913.2:n.182+7843T>C
ENST00000508426.6:c.100T>C	ENSP00000429545.1:p.Leu34=
ENST00000508794.6:n.116+7843T>C
ENST00000517649.5:c.100T>C	ENSP00000428657.1:p.Leu34=
ENST00000519014.1:c.100T>C	ENSP00000429154.1:p.Leu34=
ENST00000523981.5:c.182+7843T>C	ENSP00000428363.1:n.182+7843T>C
NM_004536.2:c.100T>C	NP_004527.2:p.Leu34=
NM_022892.1:c.182+7843T>C	NP_075043.1:n.182+7843T>C
XM_005248524.1:c.100T>C	XP_005248581.1:p.Leu34=
XM_006714626.1:c.100T>C	XP_006714689.1:p.Leu34=
XM_006714629.2:c.-125+7843T>C	XP_006714692.1:n.-125+7843T>C
XM_006714630.2:c.100T>C	XP_006714693.1:p.Leu34=
XM_011543409.1:c.100T>C	XP_011541711.1:p.Leu34=
XM_011543410.1:c.137+7843T>C	XP_011541712.1:n.137+7843T>C
XM_011543411.1:c.-528T>C	XP_011541713.1:n.-528T>C
NM_001346870.1:c.100T>C	NP_001333799.1:p.Leu34=
NM_001346870.2:c.100T>C	NP_001333799.1:p.Leu34=
NM_004536.3:c.100T>C MANE Select	NP_004527.2:p.Leu34=
NM_022892.2:c.182+7843T>C	NP_075043.1:n.182+7843T>C