Canonical Allele Identifier: CA385122288

Gene: HNRNPA1

Linked Data

• MyVariant Identifiers: chr12:g.54677628G>T (hg19) ; chr12:g.54283844G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.54283844G>T , CM000674.2:g.54283844G>T	GRCh38
NC_000012.11:g.54677628G>T , CM000674.1:g.54677628G>T	GRCh37
NC_000012.10:g.52963895G>T	NCBI36
NG_033830.1:g.8141G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340913.11:c.940G>T MANE Select	ENSP00000341826.7:p.Asp314Tyr
ENST00000550482.2:c.784G>T	ENSP00000446486.2:p.Asp262Tyr
ENST00000676472.1:c.72G>T
ENST00000676572.1:c.166G>T
ENST00000676707.1:c.87G>T
ENST00000676725.1:n.1114G>T
ENST00000676794.1:c.-42G>T	ENSP00000504819.1:n.-42G>T
ENST00000676853.1:c.168G>T
ENST00000676886.1:c.85-414G>T
ENST00000676951.1:c.189G>T
ENST00000677191.1:c.280G>T
ENST00000677210.1:c.940G>T	ENSP00000503610.1:p.Asp314Tyr
ENST00000677220.1:c.132+2342G>T	ENSP00000502987.1:n.132+2342G>T
ENST00000677224.1:c.42G>T
ENST00000677249.1:c.781G>T	ENSP00000503649.1:p.Asp261Tyr
ENST00000677279.1:c.39G>T
ENST00000677375.1:c.784G>T	ENSP00000503651.1:p.Asp262Tyr
ENST00000677385.1:c.*1126G>T	ENSP00000502985.1:n.*1126G>T
ENST00000677518.1:c.33G>T
ENST00000677539.1:c.322G>T
ENST00000677636.1:c.126G>T
ENST00000677778.1:c.75+970G>T
ENST00000677840.1:c.33G>T
ENST00000677847.1:c.24+9G>T
ENST00000677945.1:c.111G>T
ENST00000678077.1:c.649G>T	ENSP00000504814.1:p.Asp217Tyr
ENST00000678212.1:c.128G>T
ENST00000678279.1:n.67-48G>T
ENST00000678365.1:n.49-2818G>T
ENST00000678412.1:c.157-414G>T
ENST00000678418.1:n.1136G>T
ENST00000678424.1:c.165G>T
ENST00000678448.1:c.132G>T	ENSP00000503619.1:p.Met44Ile
ENST00000678456.1:c.76-414G>T
ENST00000678513.1:c.60G>T
ENST00000678581.1:c.168G>T
ENST00000678597.1:c.57G>T
ENST00000678611.1:c.174G>T
ENST00000678873.1:c.108G>T
ENST00000678876.1:c.126G>T
ENST00000678934.1:c.87G>T
ENST00000678970.1:c.157-48G>T
ENST00000679026.1:c.33G>T
ENST00000679063.1:c.108G>T
ENST00000679079.1:c.156+610G>T
ENST00000679228.1:n.1135G>T
ENST00000679273.1:c.120G>T	ENSP00000504626.1:p.Met40Ile
ENST00000679344.1:c.141G>T
ENST00000330752.12:c.745G>T	ENSP00000333504.8:p.Asp249Tyr
ENST00000340913.10:c.940G>T	ENSP00000341826.6:p.Asp314Tyr
ENST00000546500.5:c.784G>T	ENSP00000448617.1:p.Asp262Tyr
ENST00000547276.5:c.625G>T	ENSP00000447260.1:p.Asp209Tyr
ENST00000547566.5:c.784G>T	ENSP00000449913.1:p.Asp262Tyr
ENST00000547708.5:c.436G>T	ENSP00000448229.1:p.Asp146Tyr
ENST00000550482.1:c.397G>T	ENSP00000446486.1:p.Asp133Tyr
ENST00000551679.1:n.122G>T
NM_002136.2:c.784G>T	NP_002127.1:p.Asp262Tyr
NM_031157.2:c.940G>T	NP_112420.1:p.Asp314Tyr
XM_005268826.1:c.940G>T	XP_005268883.1:p.Asp314Tyr
XR_245923.1:n.1052G>T
XR_245924.1:n.896G>T
NM_002136.3:c.784G>T	NP_002127.1:p.Asp262Tyr
NM_031157.3:c.940G>T	NP_112420.1:p.Asp314Tyr
NR_135167.1:n.902G>T
XM_005268826.2:c.940G>T	XP_005268883.1:p.Asp314Tyr
XR_245923.2:n.1012G>T
NM_002136.4:c.784G>T	NP_002127.1:p.Asp262Tyr
NM_031157.4:c.940G>T MANE Select	NP_112420.1:p.Asp314Tyr
NR_135167.2:n.866G>T