Canonical Allele Identifier: CA2037357604
Gene: HNRNPA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.54283860A= , CM000674.2:g.54283860A= GRCh38
NC_000012.11:g.54677644A= , CM000674.1:g.54677644A= GRCh37
NC_000012.10:g.52963911A= NCBI36
NG_033830.1:g.8157A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000340913.11:c.956A= MANE Select ENSP00000341826.7:p.Asn319=
ENST00000550482.2:c.800A= ENSP00000446486.2:p.Asn267=
ENST00000676472.1:c.88A=
ENST00000676572.1:c.182A=
ENST00000676707.1:c.103A=
ENST00000676725.1:n.1130A=
ENST00000676794.1:c.-26A= ENSP00000504819.1:n.-26A=
ENST00000676853.1:c.184A=
ENST00000676886.1:c.85-398A=
ENST00000676951.1:c.205A=
ENST00000677191.1:c.296A=
ENST00000677210.1:c.956A= ENSP00000503610.1:p.Asn319=
ENST00000677220.1:c.132+2358A= ENSP00000502987.1:n.132+2358A=
ENST00000677224.1:c.58A=
ENST00000677249.1:c.797A= ENSP00000503649.1:p.Asn266=
ENST00000677279.1:c.55A=
ENST00000677375.1:c.800A= ENSP00000503651.1:p.Asn267=
ENST00000677385.1:c.*1142A= ENSP00000502985.1:n.*1142A=
ENST00000677518.1:c.49A=
ENST00000677539.1:c.338A=
ENST00000677636.1:c.142A=
ENST00000677778.1:c.75+986A=
ENST00000677840.1:c.49A=
ENST00000677847.1:c.24+25A=
ENST00000677945.1:c.127A=
ENST00000678077.1:c.665A= ENSP00000504814.1:p.Asn222=
ENST00000678212.1:c.144A=
ENST00000678279.1:n.67-32A=
ENST00000678365.1:n.49-2802A=
ENST00000678412.1:c.157-398A=
ENST00000678418.1:n.1152A=
ENST00000678424.1:c.181A=
ENST00000678448.1:c.148A= ENSP00000503619.1:p.Thr50=
ENST00000678456.1:c.76-398A=
ENST00000678513.1:c.76A=
ENST00000678581.1:c.184A=
ENST00000678597.1:c.73A=
ENST00000678611.1:c.190A=
ENST00000678873.1:c.124A=
ENST00000678876.1:c.142A=
ENST00000678934.1:c.103A=
ENST00000678970.1:c.157-32A=
ENST00000679026.1:c.49A=
ENST00000679063.1:c.124A=
ENST00000679079.1:c.156+626A=
ENST00000679228.1:n.1151A=
ENST00000679273.1:c.136A= ENSP00000504626.1:p.Thr46=
ENST00000679344.1:c.157A=
ENST00000330752.12:c.761A= ENSP00000333504.8:p.Asn254=
ENST00000340913.10:c.956A= ENSP00000341826.6:p.Asn319=
ENST00000546500.5:c.800A= ENSP00000448617.1:p.Asn267=
ENST00000547276.5:c.641A= ENSP00000447260.1:p.Asn214=
ENST00000547566.5:c.800A= ENSP00000449913.1:p.Asn267=
ENST00000547708.5:c.452A= ENSP00000448229.1:p.Asn151=
ENST00000550482.1:c.413A= ENSP00000446486.1:p.Asn138=
ENST00000551679.1:n.138A=
NM_002136.2:c.800A= NP_002127.1:p.Asn267=
NM_031157.2:c.956A= NP_112420.1:p.Asn319=
XM_005268826.1:c.956A= XP_005268883.1:p.Asn319=
XR_245923.1:n.1068A=
XR_245924.1:n.912A=
NM_002136.3:c.800A= NP_002127.1:p.Asn267=
NM_031157.3:c.956A= NP_112420.1:p.Asn319=
NR_135167.1:n.918A=
XM_005268826.2:c.956A= XP_005268883.1:p.Asn319=
XR_245923.2:n.1028A=
NM_002136.4:c.800A= NP_002127.1:p.Asn267=
NM_031157.4:c.956A= MANE Select NP_112420.1:p.Asn319=
NR_135167.2:n.882A=