Canonical Allele Identifier: CA359654998

Gene: NNT

Linked Data

• MyVariant Identifiers: chr5:g.43702754T>A (hg19) ; chr5:g.43702652T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.43702652T>A , CM000667.2:g.43702652T>A	GRCh38
NC_000005.9:g.43702754T>A , CM000667.1:g.43702754T>A	GRCh37
NC_000005.8:g.43738511T>A	NCBI36
NG_032869.1:g.104964T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344920.9:c.3027T>A MANE Select	ENSP00000343873.4:p.Asn1009Lys
ENST00000652986.1:c.*2333T>A	ENSP00000499801.1:n.*2333T>A
ENST00000653251.1:c.3027T>A	ENSP00000499281.1:p.Asn1009Lys
ENST00000654405.1:c.2850T>A	ENSP00000499670.1:p.Asn950Lys
ENST00000654931.1:c.*2889T>A	ENSP00000499477.1:n.*2889T>A
ENST00000656666.1:c.3027T>A	ENSP00000499249.1:p.Asn1009Lys
ENST00000657973.1:c.*3143T>A	ENSP00000499581.1:n.*3143T>A
ENST00000658729.1:c.*2592T>A	ENSP00000499331.1:n.*2592T>A
ENST00000660676.1:c.*2786T>A	ENSP00000499491.1:n.*2786T>A
ENST00000662525.1:c.3027T>A	ENSP00000499639.1:p.Asn1009Lys
ENST00000669601.1:c.3027T>A	ENSP00000499527.1:p.Asn1009Lys
ENST00000670904.1:c.3027T>A	ENSP00000499611.1:p.Asn1009Lys
ENST00000671668.1:c.3027T>A	ENSP00000499494.1:p.Asn1009Lys
ENST00000264663.9:c.3027T>A	ENSP00000264663.5:p.Asn1009Lys
ENST00000344920.8:c.3027T>A	ENSP00000343873.4:p.Asn1009Lys
ENST00000503059.1:c.60T>A
ENST00000512996.6:c.2634T>A	ENSP00000426343.1:p.Asn878Lys
NM_012343.3:c.3027T>A	NP_036475.3:p.Asn1009Lys
NM_182977.2:c.3027T>A	NP_892022.2:p.Asn1009Lys
XM_005248274.3:c.3027T>A	XP_005248331.1:p.Asn1009Lys
XM_005248275.3:c.1527T>A	XP_005248332.1:p.Asn509Lys
XM_006714461.2:c.2634T>A	XP_006714524.1:p.Asn878Lys
XM_011514001.1:c.3027T>A	XP_011512303.1:p.Asn1009Lys
XM_011514002.1:c.2634T>A	XP_011512304.1:p.Asn878Lys
NM_001331026.1:c.2634T>A	NP_001317955.1:p.Asn878Lys
XM_005248274.5:c.3027T>A	XP_005248331.1:p.Asn1009Lys
XM_005248275.5:c.1527T>A	XP_005248332.1:p.Asn509Lys
XM_006714461.4:c.2634T>A	XP_006714524.1:p.Asn878Lys
XM_011514001.3:c.3027T>A	XP_011512303.1:p.Asn1009Lys
XM_017009293.2:c.3027T>A	XP_016864782.1:p.Asn1009Lys
XM_024446009.1:c.1527T>A	XP_024301777.1:p.Asn509Lys
NM_182977.3:c.3027T>A MANE Select	NP_892022.2:p.Asn1009Lys
NM_001331026.2:c.2634T>A	NP_001317955.1:p.Asn878Lys
NM_012343.4:c.3027T>A	NP_036475.3:p.Asn1009Lys