Canonical Allele Identifier: CA385122324

Gene: HNRNPA1

Linked Data

• MyVariant Identifiers: chr12:g.54677644A>T (hg19) ; chr12:g.54283860A>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340913.11:c.956A>T MANE Select	ENSP00000341826.7:p.Asn319Ile
ENST00000550482.2:c.800A>T	ENSP00000446486.2:p.Asn267Ile
ENST00000676472.1:c.88A>T
ENST00000676572.1:c.182A>T
ENST00000676707.1:c.103A>T
ENST00000676725.1:n.1130A>T
ENST00000676794.1:c.-26A>T	ENSP00000504819.1:n.-26A>T
ENST00000676853.1:c.184A>T
ENST00000676886.1:c.85-398A>T
ENST00000676951.1:c.205A>T
ENST00000677191.1:c.296A>T
ENST00000677210.1:c.956A>T	ENSP00000503610.1:p.Asn319Ile
ENST00000677220.1:c.132+2358A>T	ENSP00000502987.1:n.132+2358A>T
ENST00000677224.1:c.58A>T
ENST00000677249.1:c.797A>T	ENSP00000503649.1:p.Asn266Ile
ENST00000677279.1:c.55A>T
ENST00000677375.1:c.800A>T	ENSP00000503651.1:p.Asn267Ile
ENST00000677385.1:c.*1142A>T	ENSP00000502985.1:n.*1142A>T
ENST00000677518.1:c.49A>T
ENST00000677539.1:c.338A>T
ENST00000677636.1:c.142A>T
ENST00000677778.1:c.75+986A>T
ENST00000677840.1:c.49A>T
ENST00000677847.1:c.24+25A>T
ENST00000677945.1:c.127A>T
ENST00000678077.1:c.665A>T	ENSP00000504814.1:p.Asn222Ile
ENST00000678212.1:c.144A>T
ENST00000678279.1:n.67-32A>T
ENST00000678365.1:n.49-2802A>T
ENST00000678412.1:c.157-398A>T
ENST00000678418.1:n.1152A>T
ENST00000678424.1:c.181A>T
ENST00000678448.1:c.148A>T	ENSP00000503619.1:p.Thr50Ser
ENST00000678456.1:c.76-398A>T
ENST00000678513.1:c.76A>T
ENST00000678581.1:c.184A>T
ENST00000678597.1:c.73A>T
ENST00000678611.1:c.190A>T
ENST00000678873.1:c.124A>T
ENST00000678876.1:c.142A>T
ENST00000678934.1:c.103A>T
ENST00000678970.1:c.157-32A>T
ENST00000679026.1:c.49A>T
ENST00000679063.1:c.124A>T
ENST00000679079.1:c.156+626A>T
ENST00000679228.1:n.1151A>T
ENST00000679273.1:c.136A>T	ENSP00000504626.1:p.Thr46Ser
ENST00000679344.1:c.157A>T
ENST00000330752.12:c.761A>T	ENSP00000333504.8:p.Asn254Ile
ENST00000340913.10:c.956A>T	ENSP00000341826.6:p.Asn319Ile
ENST00000546500.5:c.800A>T	ENSP00000448617.1:p.Asn267Ile
ENST00000547276.5:c.641A>T	ENSP00000447260.1:p.Asn214Ile
ENST00000547566.5:c.800A>T	ENSP00000449913.1:p.Asn267Ile
ENST00000547708.5:c.452A>T	ENSP00000448229.1:p.Asn151Ile
ENST00000550482.1:c.413A>T	ENSP00000446486.1:p.Asn138Ile
ENST00000551679.1:n.138A>T
NM_002136.2:c.800A>T	NP_002127.1:p.Asn267Ile
NM_031157.2:c.956A>T	NP_112420.1:p.Asn319Ile
XM_005268826.1:c.956A>T	XP_005268883.1:p.Asn319Ile
XR_245923.1:n.1068A>T
XR_245924.1:n.912A>T
NM_002136.3:c.800A>T	NP_002127.1:p.Asn267Ile
NM_031157.3:c.956A>T	NP_112420.1:p.Asn319Ile
NR_135167.1:n.918A>T
XM_005268826.2:c.956A>T	XP_005268883.1:p.Asn319Ile
XR_245923.2:n.1028A>T
NM_002136.4:c.800A>T	NP_002127.1:p.Asn267Ile
NM_031157.4:c.956A>T MANE Select	NP_112420.1:p.Asn319Ile
NR_135167.2:n.882A>T