Canonical Allele Identifier: CA385122322

Gene: HNRNPA1

Linked Data

• MyVariant Identifiers: chr12:g.54677643A>T (hg19) ; chr12:g.54283859A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.54283859A>T , CM000674.2:g.54283859A>T	GRCh38
NC_000012.11:g.54677643A>T , CM000674.1:g.54677643A>T	GRCh37
NC_000012.10:g.52963910A>T	NCBI36
NG_033830.1:g.8156A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000340913.11:c.955A>T MANE Select	ENSP00000341826.7:p.Asn319Tyr
ENST00000550482.2:c.799A>T	ENSP00000446486.2:p.Asn267Tyr
ENST00000676472.1:c.87A>T
ENST00000676572.1:c.181A>T
ENST00000676707.1:c.102A>T
ENST00000676725.1:n.1129A>T
ENST00000676794.1:c.-27A>T	ENSP00000504819.1:n.-27A>T
ENST00000676853.1:c.183A>T
ENST00000676886.1:c.85-399A>T
ENST00000676951.1:c.204A>T
ENST00000677191.1:c.295A>T
ENST00000677210.1:c.955A>T	ENSP00000503610.1:p.Asn319Tyr
ENST00000677220.1:c.132+2357A>T	ENSP00000502987.1:n.132+2357A>T
ENST00000677224.1:c.57A>T
ENST00000677249.1:c.796A>T	ENSP00000503649.1:p.Asn266Tyr
ENST00000677279.1:c.54A>T
ENST00000677375.1:c.799A>T	ENSP00000503651.1:p.Asn267Tyr
ENST00000677385.1:c.*1141A>T	ENSP00000502985.1:n.*1141A>T
ENST00000677518.1:c.48A>T
ENST00000677539.1:c.337A>T
ENST00000677636.1:c.141A>T
ENST00000677778.1:c.75+985A>T
ENST00000677840.1:c.48A>T
ENST00000677847.1:c.24+24A>T
ENST00000677945.1:c.126A>T
ENST00000678077.1:c.664A>T	ENSP00000504814.1:p.Asn222Tyr
ENST00000678212.1:c.143A>T
ENST00000678279.1:n.67-33A>T
ENST00000678365.1:n.49-2803A>T
ENST00000678412.1:c.157-399A>T
ENST00000678418.1:n.1151A>T
ENST00000678424.1:c.180A>T
ENST00000678448.1:c.147A>T	ENSP00000503619.1:p.Thr49=
ENST00000678456.1:c.76-399A>T
ENST00000678513.1:c.75A>T
ENST00000678581.1:c.183A>T
ENST00000678597.1:c.72A>T
ENST00000678611.1:c.189A>T
ENST00000678873.1:c.123A>T
ENST00000678876.1:c.141A>T
ENST00000678934.1:c.102A>T
ENST00000678970.1:c.157-33A>T
ENST00000679026.1:c.48A>T
ENST00000679063.1:c.123A>T
ENST00000679079.1:c.156+625A>T
ENST00000679228.1:n.1150A>T
ENST00000679273.1:c.135A>T	ENSP00000504626.1:p.Thr45=
ENST00000679344.1:c.156A>T
ENST00000330752.12:c.760A>T	ENSP00000333504.8:p.Asn254Tyr
ENST00000340913.10:c.955A>T	ENSP00000341826.6:p.Asn319Tyr
ENST00000546500.5:c.799A>T	ENSP00000448617.1:p.Asn267Tyr
ENST00000547276.5:c.640A>T	ENSP00000447260.1:p.Asn214Tyr
ENST00000547566.5:c.799A>T	ENSP00000449913.1:p.Asn267Tyr
ENST00000547708.5:c.451A>T	ENSP00000448229.1:p.Asn151Tyr
ENST00000550482.1:c.412A>T	ENSP00000446486.1:p.Asn138Tyr
ENST00000551679.1:n.137A>T
NM_002136.2:c.799A>T	NP_002127.1:p.Asn267Tyr
NM_031157.2:c.955A>T	NP_112420.1:p.Asn319Tyr
XM_005268826.1:c.955A>T	XP_005268883.1:p.Asn319Tyr
XR_245923.1:n.1067A>T
XR_245924.1:n.911A>T
NM_002136.3:c.799A>T	NP_002127.1:p.Asn267Tyr
NM_031157.3:c.955A>T	NP_112420.1:p.Asn319Tyr
NR_135167.1:n.917A>T
XM_005268826.2:c.955A>T	XP_005268883.1:p.Asn319Tyr
XR_245923.2:n.1027A>T
NM_002136.4:c.799A>T	NP_002127.1:p.Asn267Tyr
NM_031157.4:c.955A>T MANE Select	NP_112420.1:p.Asn319Tyr
NR_135167.2:n.881A>T