Canonical Allele Identifier: CA385122363
Gene: HNRNPA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.54283879T>A , CM000674.2:g.54283879T>A GRCh38
NC_000012.11:g.54677663T>A , CM000674.1:g.54677663T>A GRCh37
NC_000012.10:g.52963930T>A NCBI36
NG_033830.1:g.8176T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000340913.11:c.975T>A MANE Select ENSP00000341826.7:p.Phe325Leu
ENST00000550482.2:c.819T>A ENSP00000446486.2:p.Phe273Leu
ENST00000676472.1:c.107T>A
ENST00000676572.1:c.201T>A
ENST00000676707.1:c.122T>A
ENST00000676725.1:n.1149T>A
ENST00000676794.1:c.-7T>A ENSP00000504819.1:n.-7T>A
ENST00000676853.1:c.203T>A
ENST00000676886.1:c.85-379T>A
ENST00000676951.1:c.224T>A
ENST00000677191.1:c.315T>A
ENST00000677210.1:c.975T>A ENSP00000503610.1:p.Phe325Leu
ENST00000677220.1:c.132+2377T>A ENSP00000502987.1:n.132+2377T>A
ENST00000677224.1:c.77T>A
ENST00000677249.1:c.816T>A ENSP00000503649.1:p.Phe272Leu
ENST00000677279.1:c.74T>A
ENST00000677375.1:c.819T>A ENSP00000503651.1:p.Phe273Leu
ENST00000677385.1:c.*1161T>A ENSP00000502985.1:n.*1161T>A
ENST00000677518.1:c.68T>A
ENST00000677539.1:c.357T>A
ENST00000677636.1:c.161T>A
ENST00000677778.1:c.75+1005T>A
ENST00000677840.1:c.68T>A
ENST00000677847.1:c.25-17T>A
ENST00000677945.1:c.146T>A
ENST00000678077.1:c.684T>A ENSP00000504814.1:p.Phe228Leu
ENST00000678212.1:c.163T>A
ENST00000678279.1:n.67-13T>A
ENST00000678365.1:n.49-2783T>A
ENST00000678412.1:c.157-379T>A
ENST00000678418.1:n.1171T>A
ENST00000678424.1:c.200T>A
ENST00000678448.1:c.167T>A ENSP00000503619.1:p.Leu56Ter
ENST00000678456.1:c.76-379T>A
ENST00000678513.1:c.95T>A
ENST00000678581.1:c.203T>A
ENST00000678597.1:c.92T>A
ENST00000678611.1:c.209T>A
ENST00000678873.1:c.143T>A
ENST00000678876.1:c.161T>A
ENST00000678934.1:c.122T>A
ENST00000678970.1:c.157-13T>A
ENST00000679026.1:c.68T>A
ENST00000679063.1:c.143T>A
ENST00000679079.1:c.156+645T>A
ENST00000679228.1:n.1170T>A
ENST00000679273.1:c.155T>A ENSP00000504626.1:p.Leu52Ter
ENST00000679344.1:c.176T>A
ENST00000330752.12:c.780T>A ENSP00000333504.8:p.Phe260Leu
ENST00000340913.10:c.975T>A ENSP00000341826.6:p.Phe325Leu
ENST00000546500.5:c.819T>A ENSP00000448617.1:p.Phe273Leu
ENST00000547276.5:c.660T>A ENSP00000447260.1:p.Phe220Leu
ENST00000547566.5:c.819T>A ENSP00000449913.1:p.Phe273Leu
ENST00000550482.1:c.432T>A ENSP00000446486.1:p.Phe144Leu
ENST00000551679.1:n.157T>A
NM_002136.2:c.819T>A NP_002127.1:p.Phe273Leu
NM_031157.2:c.975T>A NP_112420.1:p.Phe325Leu
XM_005268826.1:c.975T>A XP_005268883.1:p.Phe325Leu
XR_245923.1:n.1087T>A
XR_245924.1:n.931T>A
NM_002136.3:c.819T>A NP_002127.1:p.Phe273Leu
NM_031157.3:c.975T>A NP_112420.1:p.Phe325Leu
NR_135167.1:n.937T>A
XM_005268826.2:c.975T>A XP_005268883.1:p.Phe325Leu
XR_245923.2:n.1047T>A
NM_002136.4:c.819T>A NP_002127.1:p.Phe273Leu
NM_031157.4:c.975T>A MANE Select NP_112420.1:p.Phe325Leu
NR_135167.2:n.901T>A