Canonical Allele Identifier: CA385122539

Gene: HNRNPA1

Linked Data

• MyVariant Identifiers: chr12:g.54677748C>G (hg19) ; chr12:g.54283964C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.54283964C>G , CM000674.2:g.54283964C>G	GRCh38
NC_000012.11:g.54677748C>G , CM000674.1:g.54677748C>G	GRCh37
NC_000012.10:g.52964015C>G	NCBI36
NG_033830.1:g.8261C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340913.11:c.1060C>G MANE Select	ENSP00000341826.7:p.Gln354Glu
ENST00000550482.2:c.904C>G	ENSP00000446486.2:p.Gln302Glu
ENST00000676472.1:c.192C>G
ENST00000676572.1:c.286C>G
ENST00000676707.1:c.207C>G
ENST00000676725.1:n.1234C>G
ENST00000676794.1:c.79C>G	ENSP00000504819.1:p.Gln27Glu
ENST00000676853.1:c.288C>G
ENST00000676886.1:c.85-294C>G
ENST00000676951.1:c.309C>G
ENST00000677191.1:c.400C>G
ENST00000677210.1:c.1060C>G	ENSP00000503610.1:p.Gln354Glu
ENST00000677220.1:c.132+2462C>G	ENSP00000502987.1:n.132+2462C>G
ENST00000677224.1:c.162C>G
ENST00000677249.1:c.901C>G	ENSP00000503649.1:p.Gln301Glu
ENST00000677279.1:c.159C>G
ENST00000677375.1:c.904C>G	ENSP00000503651.1:p.Gln302Glu
ENST00000677385.1:c.*1246C>G	ENSP00000502985.1:n.*1246C>G
ENST00000677518.1:c.123C>G
ENST00000677539.1:c.442C>G
ENST00000677636.1:c.246C>G
ENST00000677778.1:c.75+1090C>G
ENST00000677840.1:c.153C>G
ENST00000677847.1:c.93C>G
ENST00000677945.1:c.231C>G
ENST00000678077.1:c.769C>G	ENSP00000504814.1:p.Gln257Glu
ENST00000678212.1:c.248C>G
ENST00000678279.1:n.139C>G
ENST00000678365.1:n.49-2698C>G
ENST00000678412.1:c.157-294C>G
ENST00000678418.1:n.1256C>G
ENST00000678424.1:c.285C>G
ENST00000678448.1:c.252C>G	ENSP00000503619.1:n.252C>G
ENST00000678456.1:c.76-294C>G
ENST00000678513.1:c.180C>G
ENST00000678581.1:c.288C>G
ENST00000678597.1:c.177C>G
ENST00000678611.1:c.294C>G
ENST00000678873.1:c.228C>G
ENST00000678876.1:c.246C>G
ENST00000678934.1:c.207C>G
ENST00000678970.1:c.229C>G
ENST00000679026.1:c.153C>G
ENST00000679063.1:c.228C>G
ENST00000679079.1:c.157-585C>G
ENST00000679228.1:n.1255C>G
ENST00000679273.1:c.240C>G	ENSP00000504626.1:n.240C>G
ENST00000679344.1:c.261C>G
ENST00000330752.12:c.865C>G	ENSP00000333504.8:p.Gln289Glu
ENST00000340913.10:c.1060C>G	ENSP00000341826.6:p.Gln354Glu
ENST00000546500.5:c.904C>G	ENSP00000448617.1:p.Gln302Glu
ENST00000547276.5:c.745C>G	ENSP00000447260.1:p.Gln249Glu
ENST00000547566.5:c.904C>G	ENSP00000449913.1:p.Gln302Glu
ENST00000550482.1:c.517C>G	ENSP00000446486.1:p.Gln173Glu
ENST00000551679.1:n.242C>G
NM_002136.2:c.904C>G	NP_002127.1:p.Gln302Glu
NM_031157.2:c.1060C>G	NP_112420.1:p.Gln354Glu
XM_005268826.1:c.1060C>G	XP_005268883.1:p.Gln354Glu
XR_245923.1:n.1172C>G
XR_245924.1:n.1016C>G
NM_002136.3:c.904C>G	NP_002127.1:p.Gln302Glu
NM_031157.3:c.1060C>G	NP_112420.1:p.Gln354Glu
NR_135167.1:n.1022C>G
XM_005268826.2:c.1060C>G	XP_005268883.1:p.Gln354Glu
XR_245923.2:n.1132C>G
NM_002136.4:c.904C>G	NP_002127.1:p.Gln302Glu
NM_031157.4:c.1060C>G MANE Select	NP_112420.1:p.Gln354Glu
NR_135167.2:n.986C>G