Canonical Allele Identifier: CA385122291

Gene: HNRNPA1

Linked Data

• MyVariant Identifiers: chr12:g.54677630T>A (hg19) ; chr12:g.54283846T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.54283846T>A , CM000674.2:g.54283846T>A	GRCh38
NC_000012.11:g.54677630T>A , CM000674.1:g.54677630T>A	GRCh37
NC_000012.10:g.52963897T>A	NCBI36
NG_033830.1:g.8143T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000340913.11:c.942T>A MANE Select	ENSP00000341826.7:p.Asp314Glu
ENST00000550482.2:c.786T>A	ENSP00000446486.2:p.Asp262Glu
ENST00000676472.1:c.74T>A
ENST00000676572.1:c.168T>A
ENST00000676707.1:c.89T>A
ENST00000676725.1:n.1116T>A
ENST00000676794.1:c.-40T>A	ENSP00000504819.1:n.-40T>A
ENST00000676853.1:c.170T>A
ENST00000676886.1:c.85-412T>A
ENST00000676951.1:c.191T>A
ENST00000677191.1:c.282T>A
ENST00000677210.1:c.942T>A	ENSP00000503610.1:p.Asp314Glu
ENST00000677220.1:c.132+2344T>A	ENSP00000502987.1:n.132+2344T>A
ENST00000677224.1:c.44T>A
ENST00000677249.1:c.783T>A	ENSP00000503649.1:p.Asp261Glu
ENST00000677279.1:c.41T>A
ENST00000677375.1:c.786T>A	ENSP00000503651.1:p.Asp262Glu
ENST00000677385.1:c.*1128T>A	ENSP00000502985.1:n.*1128T>A
ENST00000677518.1:c.35T>A
ENST00000677539.1:c.324T>A
ENST00000677636.1:c.128T>A
ENST00000677778.1:c.75+972T>A
ENST00000677840.1:c.35T>A
ENST00000677847.1:c.24+11T>A
ENST00000677945.1:c.113T>A
ENST00000678077.1:c.651T>A	ENSP00000504814.1:p.Asp217Glu
ENST00000678212.1:c.130T>A
ENST00000678279.1:n.67-46T>A
ENST00000678365.1:n.49-2816T>A
ENST00000678412.1:c.157-412T>A
ENST00000678418.1:n.1138T>A
ENST00000678424.1:c.167T>A
ENST00000678448.1:c.134T>A	ENSP00000503619.1:p.Ile45Asn
ENST00000678456.1:c.76-412T>A
ENST00000678513.1:c.62T>A
ENST00000678581.1:c.170T>A
ENST00000678597.1:c.59T>A
ENST00000678611.1:c.176T>A
ENST00000678873.1:c.110T>A
ENST00000678876.1:c.128T>A
ENST00000678934.1:c.89T>A
ENST00000678970.1:c.157-46T>A
ENST00000679026.1:c.35T>A
ENST00000679063.1:c.110T>A
ENST00000679079.1:c.156+612T>A
ENST00000679228.1:n.1137T>A
ENST00000679273.1:c.122T>A	ENSP00000504626.1:p.Ile41Asn
ENST00000679344.1:c.143T>A
ENST00000330752.12:c.747T>A	ENSP00000333504.8:p.Asp249Glu
ENST00000340913.10:c.942T>A	ENSP00000341826.6:p.Asp314Glu
ENST00000546500.5:c.786T>A	ENSP00000448617.1:p.Asp262Glu
ENST00000547276.5:c.627T>A	ENSP00000447260.1:p.Asp209Glu
ENST00000547566.5:c.786T>A	ENSP00000449913.1:p.Asp262Glu
ENST00000547708.5:c.438T>A	ENSP00000448229.1:p.Asp146Glu
ENST00000550482.1:c.399T>A	ENSP00000446486.1:p.Asp133Glu
ENST00000551679.1:n.124T>A
NM_002136.2:c.786T>A	NP_002127.1:p.Asp262Glu
NM_031157.2:c.942T>A	NP_112420.1:p.Asp314Glu
XM_005268826.1:c.942T>A	XP_005268883.1:p.Asp314Glu
XR_245923.1:n.1054T>A
XR_245924.1:n.898T>A
NM_002136.3:c.786T>A	NP_002127.1:p.Asp262Glu
NM_031157.3:c.942T>A	NP_112420.1:p.Asp314Glu
NR_135167.1:n.904T>A
XM_005268826.2:c.942T>A	XP_005268883.1:p.Asp314Glu
XR_245923.2:n.1014T>A
NM_002136.4:c.786T>A	NP_002127.1:p.Asp262Glu
NM_031157.4:c.942T>A MANE Select	NP_112420.1:p.Asp314Glu
NR_135167.2:n.868T>A