Canonical Allele Identifier: CA1309939813

Gene: HNRNPA3 NFE2L2

Linked Data

• dbSNP Id: rs2588882

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.177222437G>C , CM000664.2:g.177222437G>C	GRCh38
NC_000002.11:g.178087165G>C , CM000664.1:g.178087165G>C	GRCh37
NC_000002.10:g.177795411G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000392524.7:c.*3045G>C (HNRNPA3) MANE Select	ENSP00000376309.2:n.*3045G>C
ENST00000699220.1:c.*82C>G (NFE2L2)	ENSP00000514214.1:n.*82C>G
ENST00000699296.1:c.704+86C>G (NFE2L2)	ENSP00000514276.1:n.704+86C>G
ENST00000699297.1:c.*82C>G (NFE2L2)	ENSP00000514277.1:n.*82C>G
ENST00000699342.1:c.824+86C>G (NFE2L2)	ENSP00000514317.1:n.824+86C>G
ENST00000699404.1:c.821+86C>G (NFE2L2)	ENSP00000514365.1:n.821+86C>G
ENST00000699405.1:c.*82C>G (NFE2L2)	ENSP00000514366.1:n.*82C>G
ENST00000699431.1:c.776+86C>G (NFE2L2)	ENSP00000514384.1:n.776+86C>G
ENST00000699432.1:c.732+86C>G (NFE2L2)	ENSP00000514385.1:n.732+86C>G
ENST00000483137.2:n.4640G>C (HNRNPA3)
ENST00000676488.1:c.*2962G>C (HNRNPA3)	ENSP00000503067.1:n.*2962G>C
ENST00000676629.1:c.*3055G>C (HNRNPA3)	ENSP00000503593.1:n.*3055G>C
ENST00000676681.1:c.*3045G>C (HNRNPA3)	ENSP00000503339.1:n.*3045G>C
ENST00000676736.1:c.*3045G>C (HNRNPA3)	ENSP00000503729.1:n.*3045G>C
ENST00000676762.1:n.4726G>C (HNRNPA3)
ENST00000676874.1:c.*393G>C (HNRNPA3)	ENSP00000503186.1:n.*393G>C
ENST00000677043.1:c.*393G>C (HNRNPA3)	ENSP00000504649.1:n.*393G>C
ENST00000677337.1:c.*2962G>C (HNRNPA3)	ENSP00000504054.1:n.*2962G>C
ENST00000677508.1:n.4470G>C (HNRNPA3)
ENST00000677863.1:c.*3045G>C (HNRNPA3)	ENSP00000504218.1:n.*3045G>C
ENST00000678111.1:c.*393G>C (HNRNPA3)	ENSP00000504135.1:n.*393G>C
ENST00000678421.1:n.4346G>C (HNRNPA3)
ENST00000679159.1:c.*2962G>C (HNRNPA3)	ENSP00000504152.1:n.*2962G>C
ENST00000411529.6:c.*3045G>C (HNRNPA3)	ENSP00000408487.1:n.*3045G>C
NM_194247.2:c.*3045G>C (HNRNPA3)	NP_919223.1:n.*3045G>C
XM_005246380.1:c.*393G>C (HNRNPA3)	XP_005246437.1:n.*393G>C
XM_011512283.1:c.-2+4204C>G	XP_011510585.1:n.-2+4204C>G
NM_001330247.1:c.*3045G>C (HNRNPA3)	NP_001317176.1:n.*3045G>C
NM_001330248.1:c.*393G>C (HNRNPA3)	NP_001317177.1:n.*393G>C
NM_001330249.1:c.*393G>C (HNRNPA3)	NP_001317178.1:n.*393G>C
NM_001330250.1:c.*393G>C (HNRNPA3)	NP_001317179.1:n.*393G>C
NM_001330251.1:c.*3045G>C (HNRNPA3)	NP_001317180.1:n.*3045G>C
NM_194247.3:c.*3045G>C (HNRNPA3)	NP_919223.1:n.*3045G>C
NR_138470.1:n.4205G>C (HNRNPA3)
NR_138470.2:n.4105G>C (HNRNPA3)
NM_001330247.2:c.*3045G>C (HNRNPA3)	NP_001317176.1:n.*3045G>C
NM_001330248.2:c.*393G>C (HNRNPA3)	NP_001317177.1:n.*393G>C
NM_001330249.2:c.*393G>C (HNRNPA3)	NP_001317178.1:n.*393G>C
NM_001330250.2:c.*393G>C (HNRNPA3)	NP_001317179.1:n.*393G>C
NM_001330251.2:c.*3045G>C (HNRNPA3)	NP_001317180.1:n.*3045G>C
NM_001395170.1:c.*393G>C (HNRNPA3)	NP_001382099.1:n.*393G>C
NM_194247.4:c.*3045G>C (HNRNPA3) MANE Select	NP_919223.1:n.*3045G>C