Canonical Allele Identifier: CA2335812

Gene: NKTR ZBTB47-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.42638565G>A , CM000665.2:g.42638565G>A	GRCh38
NC_000003.11:g.42680057G>A , CM000665.1:g.42680057G>A	GRCh37
NC_000003.10:g.42655061G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_005385.4:c.2861G>A (NKTR) MANE Select	NP_005376.2:p.Arg954His
ENST00000232978.13:c.2861G>A (NKTR) MANE Select	ENSP00000232978.8:p.Arg954His
NM_001349124.1:c.2861G>A (NKTR)	NP_001336053.1:p.Arg954His
NM_001349124.2:c.2861G>A (NKTR)	NP_001336053.1:p.Arg954His
NM_001349125.1:c.2102G>A (NKTR)	NP_001336054.1:p.Arg701His
NM_001349125.2:c.2102G>A (NKTR)	NP_001336054.1:p.Arg701His
NM_001349126.1:c.1757G>A (NKTR)	NP_001336055.1:p.Arg586His
NM_001349126.2:c.1757G>A (NKTR)	NP_001336055.1:p.Arg586His
NM_005385.3:c.2861G>A (NKTR)	NP_005376.2:p.Arg954His
NR_125400.1:n.396-14753C>T (ZBTB47-AS1)
ENST00000232978.12:c.2861G>A (NKTR)	ENSP00000232978.8:p.Arg954His
ENST00000429888.5:c.*2599G>A (NKTR)	ENSP00000404802.1:n.*2599G>A
ENST00000617821.4:c.1961G>A (NKTR)	ENSP00000482143.1:p.Arg654His
XM_005265173.1:c.2861G>A (NKTR)	XP_005265230.1:p.Arg954His
XM_006713171.1:c.2861G>A (NKTR)	XP_006713234.1:p.Arg954His
XM_006713171.2:c.2861G>A (NKTR)	XP_006713234.1:p.Arg954His
XM_006713173.1:c.2531G>A (NKTR)	XP_006713236.1:p.Arg844His
XM_006713173.2:c.2531G>A (NKTR)	XP_006713236.1:p.Arg844His
XM_006713174.1:c.2531G>A (NKTR)	XP_006713237.1:p.Arg844His
XM_011533746.1:c.2102G>A (NKTR)	XP_011532048.1:p.Arg701His
XM_011533747.1:c.2102G>A (NKTR)	XP_011532049.1:p.Arg701His
XM_011533747.3:c.2102G>A (NKTR)	XP_011532049.1:p.Arg701His
XM_011533748.1:c.2102G>A (NKTR)	XP_011532050.1:p.Arg701His
XM_011533749.1:c.2102G>A (NKTR)	XP_011532051.1:p.Arg701His
XM_011533750.1:c.2102G>A (NKTR)	XP_011532052.1:p.Arg701His
XM_017006474.2:c.2861G>A (NKTR)	XP_016861963.1:p.Arg954His
XM_017006475.1:c.2102G>A (NKTR)	XP_016861964.1:p.Arg701His
XM_017006476.2:c.1961G>A (NKTR)	XP_016861965.1:p.Arg654His
XM_017006477.2:c.1961G>A (NKTR)	XP_016861966.1:p.Arg654His
XM_024453539.1:c.2861G>A (NKTR)	XP_024309307.1:p.Arg954His
XM_024453540.1:c.2531G>A (NKTR)	XP_024309308.1:p.Arg844His
XM_024453541.1:c.2102G>A (NKTR)	XP_024309309.1:p.Arg701His
XM_024453543.1:c.1757G>A (NKTR)	XP_024309311.1:p.Arg586His
XM_024453544.1:c.1757G>A (NKTR)	XP_024309312.1:p.Arg586His
XM_024453545.1:c.1757G>A (NKTR)	XP_024309313.1:p.Arg586His
XR_002959537.1:n.4258G>A (NKTR)
XR_940429.2:n.2999G>A (NKTR)