Canonical Allele Identifier: CA2037357596
Gene: HNRNPA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.54283858C= , CM000674.2:g.54283858C= GRCh38
NC_000012.11:g.54677642C= , CM000674.1:g.54677642C= GRCh37
NC_000012.10:g.52963909C= NCBI36
NG_033830.1:g.8155C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000340913.11:c.954C= MANE Select ENSP00000341826.7:p.Tyr318=
ENST00000550482.2:c.798C= ENSP00000446486.2:p.Tyr266=
ENST00000676472.1:c.86C=
ENST00000676572.1:c.180C=
ENST00000676707.1:c.101C=
ENST00000676725.1:n.1128C=
ENST00000676794.1:c.-28C= ENSP00000504819.1:n.-28C=
ENST00000676853.1:c.182C=
ENST00000676886.1:c.85-400C=
ENST00000676951.1:c.203C=
ENST00000677191.1:c.294C=
ENST00000677210.1:c.954C= ENSP00000503610.1:p.Tyr318=
ENST00000677220.1:c.132+2356C= ENSP00000502987.1:n.132+2356C=
ENST00000677224.1:c.56C=
ENST00000677249.1:c.795C= ENSP00000503649.1:p.Tyr265=
ENST00000677279.1:c.53C=
ENST00000677375.1:c.798C= ENSP00000503651.1:p.Tyr266=
ENST00000677385.1:c.*1140C= ENSP00000502985.1:n.*1140C=
ENST00000677518.1:c.47C=
ENST00000677539.1:c.336C=
ENST00000677636.1:c.140C=
ENST00000677778.1:c.75+984C=
ENST00000677840.1:c.47C=
ENST00000677847.1:c.24+23C=
ENST00000677945.1:c.125C=
ENST00000678077.1:c.663C= ENSP00000504814.1:p.Tyr221=
ENST00000678212.1:c.142C=
ENST00000678279.1:n.67-34C=
ENST00000678365.1:n.49-2804C=
ENST00000678412.1:c.157-400C=
ENST00000678418.1:n.1150C=
ENST00000678424.1:c.179C=
ENST00000678448.1:c.146C= ENSP00000503619.1:p.Thr49=
ENST00000678456.1:c.76-400C=
ENST00000678513.1:c.74C=
ENST00000678581.1:c.182C=
ENST00000678597.1:c.71C=
ENST00000678611.1:c.188C=
ENST00000678873.1:c.122C=
ENST00000678876.1:c.140C=
ENST00000678934.1:c.101C=
ENST00000678970.1:c.157-34C=
ENST00000679026.1:c.47C=
ENST00000679063.1:c.122C=
ENST00000679079.1:c.156+624C=
ENST00000679228.1:n.1149C=
ENST00000679273.1:c.134C= ENSP00000504626.1:p.Thr45=
ENST00000679344.1:c.155C=
ENST00000330752.12:c.759C= ENSP00000333504.8:p.Tyr253=
ENST00000340913.10:c.954C= ENSP00000341826.6:p.Tyr318=
ENST00000546500.5:c.798C= ENSP00000448617.1:p.Tyr266=
ENST00000547276.5:c.639C= ENSP00000447260.1:p.Tyr213=
ENST00000547566.5:c.798C= ENSP00000449913.1:p.Tyr266=
ENST00000547708.5:c.450C= ENSP00000448229.1:p.Tyr150=
ENST00000550482.1:c.411C= ENSP00000446486.1:p.Tyr137=
ENST00000551679.1:n.136C=
NM_002136.2:c.798C= NP_002127.1:p.Tyr266=
NM_031157.2:c.954C= NP_112420.1:p.Tyr318=
XM_005268826.1:c.954C= XP_005268883.1:p.Tyr318=
XR_245923.1:n.1066C=
XR_245924.1:n.910C=
NM_002136.3:c.798C= NP_002127.1:p.Tyr266=
NM_031157.3:c.954C= NP_112420.1:p.Tyr318=
NR_135167.1:n.916C=
XM_005268826.2:c.954C= XP_005268883.1:p.Tyr318=
XR_245923.2:n.1026C=
NM_002136.4:c.798C= NP_002127.1:p.Tyr266=
NM_031157.4:c.954C= MANE Select NP_112420.1:p.Tyr318=
NR_135167.2:n.880C=