Canonical Allele Identifier: CA385122312

Gene: HNRNPA1

Linked Data

• MyVariant Identifiers: chr12:g.54677640T>A (hg19) ; chr12:g.54283856T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.54283856T>A , CM000674.2:g.54283856T>A	GRCh38
NC_000012.11:g.54677640T>A , CM000674.1:g.54677640T>A	GRCh37
NC_000012.10:g.52963907T>A	NCBI36
NG_033830.1:g.8153T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000340913.11:c.952T>A MANE Select	ENSP00000341826.7:p.Tyr318Asn
ENST00000550482.2:c.796T>A	ENSP00000446486.2:p.Tyr266Asn
ENST00000676472.1:c.84T>A
ENST00000676572.1:c.178T>A
ENST00000676707.1:c.99T>A
ENST00000676725.1:n.1126T>A
ENST00000676794.1:c.-30T>A	ENSP00000504819.1:n.-30T>A
ENST00000676853.1:c.180T>A
ENST00000676886.1:c.85-402T>A
ENST00000676951.1:c.201T>A
ENST00000677191.1:c.292T>A
ENST00000677210.1:c.952T>A	ENSP00000503610.1:p.Tyr318Asn
ENST00000677220.1:c.132+2354T>A	ENSP00000502987.1:n.132+2354T>A
ENST00000677224.1:c.54T>A
ENST00000677249.1:c.793T>A	ENSP00000503649.1:p.Tyr265Asn
ENST00000677279.1:c.51T>A
ENST00000677375.1:c.796T>A	ENSP00000503651.1:p.Tyr266Asn
ENST00000677385.1:c.*1138T>A	ENSP00000502985.1:n.*1138T>A
ENST00000677518.1:c.45T>A
ENST00000677539.1:c.334T>A
ENST00000677636.1:c.138T>A
ENST00000677778.1:c.75+982T>A
ENST00000677840.1:c.45T>A
ENST00000677847.1:c.24+21T>A
ENST00000677945.1:c.123T>A
ENST00000678077.1:c.661T>A	ENSP00000504814.1:p.Tyr221Asn
ENST00000678212.1:c.140T>A
ENST00000678279.1:n.67-36T>A
ENST00000678365.1:n.49-2806T>A
ENST00000678412.1:c.157-402T>A
ENST00000678418.1:n.1148T>A
ENST00000678424.1:c.177T>A
ENST00000678448.1:c.144T>A	ENSP00000503619.1:p.Ile48=
ENST00000678456.1:c.76-402T>A
ENST00000678513.1:c.72T>A
ENST00000678581.1:c.180T>A
ENST00000678597.1:c.69T>A
ENST00000678611.1:c.186T>A
ENST00000678873.1:c.120T>A
ENST00000678876.1:c.138T>A
ENST00000678934.1:c.99T>A
ENST00000678970.1:c.157-36T>A
ENST00000679026.1:c.45T>A
ENST00000679063.1:c.120T>A
ENST00000679079.1:c.156+622T>A
ENST00000679228.1:n.1147T>A
ENST00000679273.1:c.132T>A	ENSP00000504626.1:p.Ile44=
ENST00000679344.1:c.153T>A
ENST00000330752.12:c.757T>A	ENSP00000333504.8:p.Tyr253Asn
ENST00000340913.10:c.952T>A	ENSP00000341826.6:p.Tyr318Asn
ENST00000546500.5:c.796T>A	ENSP00000448617.1:p.Tyr266Asn
ENST00000547276.5:c.637T>A	ENSP00000447260.1:p.Tyr213Asn
ENST00000547566.5:c.796T>A	ENSP00000449913.1:p.Tyr266Asn
ENST00000547708.5:c.448T>A	ENSP00000448229.1:p.Tyr150Asn
ENST00000550482.1:c.409T>A	ENSP00000446486.1:p.Tyr137Asn
ENST00000551679.1:n.134T>A
NM_002136.2:c.796T>A	NP_002127.1:p.Tyr266Asn
NM_031157.2:c.952T>A	NP_112420.1:p.Tyr318Asn
XM_005268826.1:c.952T>A	XP_005268883.1:p.Tyr318Asn
XR_245923.1:n.1064T>A
XR_245924.1:n.908T>A
NM_002136.3:c.796T>A	NP_002127.1:p.Tyr266Asn
NM_031157.3:c.952T>A	NP_112420.1:p.Tyr318Asn
NR_135167.1:n.914T>A
XM_005268826.2:c.952T>A	XP_005268883.1:p.Tyr318Asn
XR_245923.2:n.1024T>A
NM_002136.4:c.796T>A	NP_002127.1:p.Tyr266Asn
NM_031157.4:c.952T>A MANE Select	NP_112420.1:p.Tyr318Asn
NR_135167.2:n.878T>A