Canonical Allele Identifier: CA385122415

Gene: HNRNPA1

Linked Data

• MyVariant Identifiers: chr12:g.54677687T>A (hg19) ; chr12:g.54283903T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.54283903T>A , CM000674.2:g.54283903T>A	GRCh38
NC_000012.11:g.54677687T>A , CM000674.1:g.54677687T>A	GRCh37
NC_000012.10:g.52963954T>A	NCBI36
NG_033830.1:g.8200T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340913.11:c.999T>A MANE Select	ENSP00000341826.7:p.Phe333Leu
ENST00000550482.2:c.843T>A	ENSP00000446486.2:p.Phe281Leu
ENST00000676472.1:c.131T>A
ENST00000676572.1:c.225T>A
ENST00000676707.1:c.146T>A
ENST00000676725.1:n.1173T>A
ENST00000676794.1:c.18T>A	ENSP00000504819.1:p.Phe6Leu
ENST00000676853.1:c.227T>A
ENST00000676886.1:c.85-355T>A
ENST00000676951.1:c.248T>A
ENST00000677191.1:c.339T>A
ENST00000677210.1:c.999T>A	ENSP00000503610.1:p.Phe333Leu
ENST00000677220.1:c.132+2401T>A	ENSP00000502987.1:n.132+2401T>A
ENST00000677224.1:c.101T>A
ENST00000677249.1:c.840T>A	ENSP00000503649.1:p.Phe280Leu
ENST00000677279.1:c.98T>A
ENST00000677375.1:c.843T>A	ENSP00000503651.1:p.Phe281Leu
ENST00000677385.1:c.*1185T>A	ENSP00000502985.1:n.*1185T>A
ENST00000677518.1:c.92T>A
ENST00000677539.1:c.381T>A
ENST00000677636.1:c.185T>A
ENST00000677778.1:c.75+1029T>A
ENST00000677840.1:c.92T>A
ENST00000677847.1:c.32T>A
ENST00000677945.1:c.170T>A
ENST00000678077.1:c.708T>A	ENSP00000504814.1:p.Phe236Leu
ENST00000678212.1:c.187T>A
ENST00000678279.1:n.78T>A
ENST00000678365.1:n.49-2759T>A
ENST00000678412.1:c.157-355T>A
ENST00000678418.1:n.1195T>A
ENST00000678424.1:c.224T>A
ENST00000678448.1:c.191T>A	ENSP00000503619.1:n.191T>A
ENST00000678456.1:c.76-355T>A
ENST00000678513.1:c.119T>A
ENST00000678581.1:c.227T>A
ENST00000678597.1:c.116T>A
ENST00000678611.1:c.233T>A
ENST00000678873.1:c.167T>A
ENST00000678876.1:c.185T>A
ENST00000678934.1:c.146T>A
ENST00000678970.1:c.168T>A
ENST00000679026.1:c.92T>A
ENST00000679063.1:c.167T>A
ENST00000679079.1:c.157-646T>A
ENST00000679228.1:n.1194T>A
ENST00000679273.1:c.179T>A	ENSP00000504626.1:n.179T>A
ENST00000679344.1:c.200T>A
ENST00000330752.12:c.804T>A	ENSP00000333504.8:p.Phe268Leu
ENST00000340913.10:c.999T>A	ENSP00000341826.6:p.Phe333Leu
ENST00000546500.5:c.843T>A	ENSP00000448617.1:p.Phe281Leu
ENST00000547276.5:c.684T>A	ENSP00000447260.1:p.Phe228Leu
ENST00000547566.5:c.843T>A	ENSP00000449913.1:p.Phe281Leu
ENST00000550482.1:c.456T>A	ENSP00000446486.1:p.Phe152Leu
ENST00000551679.1:n.181T>A
NM_002136.2:c.843T>A	NP_002127.1:p.Phe281Leu
NM_031157.2:c.999T>A	NP_112420.1:p.Phe333Leu
XM_005268826.1:c.999T>A	XP_005268883.1:p.Phe333Leu
XR_245923.1:n.1111T>A
XR_245924.1:n.955T>A
NM_002136.3:c.843T>A	NP_002127.1:p.Phe281Leu
NM_031157.3:c.999T>A	NP_112420.1:p.Phe333Leu
NR_135167.1:n.961T>A
XM_005268826.2:c.999T>A	XP_005268883.1:p.Phe333Leu
XR_245923.2:n.1071T>A
NM_002136.4:c.843T>A	NP_002127.1:p.Phe281Leu
NM_031157.4:c.999T>A MANE Select	NP_112420.1:p.Phe333Leu
NR_135167.2:n.925T>A