Canonical Allele Identifier: CA2037357806
Community Standard Title: NM_031157.4(HNRNPA1):c.1042T= (p.Phe348=)
Gene: HNRNPA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.54283946T= , CM000674.2:g.54283946T= GRCh38
NC_000012.11:g.54677730T= , CM000674.1:g.54677730T= GRCh37
NC_000012.10:g.52963997T= NCBI36
NG_033830.1:g.8243T=

Transcript Alleles

HGVS Amino-acid Change
NM_031157.4:c.1042T= MANE Select NP_112420.1:p.Phe348=
ENST00000340913.11:c.1042T= MANE Select ENSP00000341826.7:p.Phe348=
NM_002136.2:c.886T= NP_002127.1:p.Phe296=
NM_002136.3:c.886T= NP_002127.1:p.Phe296=
NM_002136.4:c.886T= NP_002127.1:p.Phe296=
NM_031157.2:c.1042T= NP_112420.1:p.Phe348=
NM_031157.3:c.1042T= NP_112420.1:p.Phe348=
NR_135167.1:n.1004T=
NR_135167.2:n.968T=
ENST00000330752.12:c.847T= ENSP00000333504.8:p.Phe283=
ENST00000340913.10:c.1042T= ENSP00000341826.6:p.Phe348=
ENST00000546500.5:c.886T= ENSP00000448617.1:p.Phe296=
ENST00000547276.5:c.727T= ENSP00000447260.1:p.Phe243=
ENST00000547566.5:c.886T= ENSP00000449913.1:p.Phe296=
ENST00000550482.1:c.499T= ENSP00000446486.1:p.Phe167=
ENST00000550482.2:c.886T= ENSP00000446486.2:p.Phe296=
ENST00000551679.1:n.224T=
ENST00000676472.1:c.174T=
ENST00000676572.1:c.268T=
ENST00000676707.1:c.189T=
ENST00000676725.1:n.1216T=
ENST00000676794.1:c.61T= ENSP00000504819.1:p.Phe21=
ENST00000676853.1:c.270T=
ENST00000676886.1:c.85-312T=
ENST00000676951.1:c.291T=
ENST00000677191.1:c.382T=
ENST00000677210.1:c.1042T= ENSP00000503610.1:p.Phe348=
ENST00000677220.1:c.132+2444T= ENSP00000502987.1:n.132+2444T=
ENST00000677224.1:c.144T=
ENST00000677249.1:c.883T= ENSP00000503649.1:p.Phe295=
ENST00000677279.1:c.141T=
ENST00000677375.1:c.886T= ENSP00000503651.1:p.Phe296=
ENST00000677385.1:c.*1228T= ENSP00000502985.1:n.*1228T=
ENST00000677518.1:c.105T=
ENST00000677539.1:c.424T=
ENST00000677636.1:c.228T=
ENST00000677778.1:c.75+1072T=
ENST00000677840.1:c.135T=
ENST00000677847.1:c.75T=
ENST00000677945.1:c.213T=
ENST00000678077.1:c.751T= ENSP00000504814.1:p.Phe251=
ENST00000678212.1:c.230T=
ENST00000678279.1:n.121T=
ENST00000678365.1:n.49-2716T=
ENST00000678412.1:c.157-312T=
ENST00000678418.1:n.1238T=
ENST00000678424.1:c.267T=
ENST00000678448.1:c.234T= ENSP00000503619.1:n.234T=
ENST00000678456.1:c.76-312T=
ENST00000678513.1:c.162T=
ENST00000678581.1:c.270T=
ENST00000678597.1:c.159T=
ENST00000678611.1:c.276T=
ENST00000678873.1:c.210T=
ENST00000678876.1:c.228T=
ENST00000678934.1:c.189T=
ENST00000678970.1:c.211T=
ENST00000679026.1:c.135T=
ENST00000679063.1:c.210T=
ENST00000679079.1:c.157-603T=
ENST00000679228.1:n.1237T=
ENST00000679273.1:c.222T= ENSP00000504626.1:n.222T=
ENST00000679344.1:c.243T=
XM_005268826.1:c.1042T= XP_005268883.1:p.Phe348=
XM_005268826.2:c.1042T= XP_005268883.1:p.Phe348=
XR_245923.1:n.1154T=
XR_245923.2:n.1114T=
XR_245924.1:n.998T=