Canonical Allele Identifier: CA385122543

Gene: HNRNPA1

Linked Data

• MyVariant Identifiers: chr12:g.54677749A>T (hg19) ; chr12:g.54283965A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.54283965A>T , CM000674.2:g.54283965A>T	GRCh38
NC_000012.11:g.54677749A>T , CM000674.1:g.54677749A>T	GRCh37
NC_000012.10:g.52964016A>T	NCBI36
NG_033830.1:g.8262A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000340913.11:c.1061A>T MANE Select	ENSP00000341826.7:p.Gln354Leu
ENST00000550482.2:c.905A>T	ENSP00000446486.2:p.Gln302Leu
ENST00000676472.1:c.193A>T
ENST00000676572.1:c.287A>T
ENST00000676707.1:c.208A>T
ENST00000676725.1:n.1235A>T
ENST00000676794.1:c.80A>T	ENSP00000504819.1:p.Gln27Leu
ENST00000676853.1:c.289A>T
ENST00000676886.1:c.85-293A>T
ENST00000676951.1:c.310A>T
ENST00000677191.1:c.401A>T
ENST00000677210.1:c.1061A>T	ENSP00000503610.1:p.Gln354Leu
ENST00000677220.1:c.132+2463A>T	ENSP00000502987.1:n.132+2463A>T
ENST00000677224.1:c.163A>T
ENST00000677249.1:c.902A>T	ENSP00000503649.1:p.Gln301Leu
ENST00000677279.1:c.160A>T
ENST00000677375.1:c.905A>T	ENSP00000503651.1:p.Gln302Leu
ENST00000677385.1:c.*1247A>T	ENSP00000502985.1:n.*1247A>T
ENST00000677518.1:c.124A>T
ENST00000677539.1:c.443A>T
ENST00000677636.1:c.247A>T
ENST00000677778.1:c.75+1091A>T
ENST00000677840.1:c.154A>T
ENST00000677847.1:c.94A>T
ENST00000677945.1:c.232A>T
ENST00000678077.1:c.770A>T	ENSP00000504814.1:p.Gln257Leu
ENST00000678212.1:c.249A>T
ENST00000678279.1:n.140A>T
ENST00000678365.1:n.49-2697A>T
ENST00000678412.1:c.157-293A>T
ENST00000678418.1:n.1257A>T
ENST00000678424.1:c.286A>T
ENST00000678448.1:c.253A>T	ENSP00000503619.1:n.253A>T
ENST00000678456.1:c.76-293A>T
ENST00000678513.1:c.181A>T
ENST00000678581.1:c.289A>T
ENST00000678597.1:c.178A>T
ENST00000678611.1:c.295A>T
ENST00000678873.1:c.229A>T
ENST00000678876.1:c.247A>T
ENST00000678934.1:c.208A>T
ENST00000678970.1:c.230A>T
ENST00000679026.1:c.154A>T
ENST00000679063.1:c.229A>T
ENST00000679079.1:c.157-584A>T
ENST00000679228.1:n.1256A>T
ENST00000679273.1:c.241A>T	ENSP00000504626.1:n.241A>T
ENST00000679344.1:c.262A>T
ENST00000330752.12:c.866A>T	ENSP00000333504.8:p.Gln289Leu
ENST00000340913.10:c.1061A>T	ENSP00000341826.6:p.Gln354Leu
ENST00000546500.5:c.905A>T	ENSP00000448617.1:p.Gln302Leu
ENST00000547276.5:c.746A>T	ENSP00000447260.1:p.Gln249Leu
ENST00000547566.5:c.905A>T	ENSP00000449913.1:p.Gln302Leu
ENST00000550482.1:c.518A>T	ENSP00000446486.1:p.Gln173Leu
ENST00000551679.1:n.243A>T
NM_002136.2:c.905A>T	NP_002127.1:p.Gln302Leu
NM_031157.2:c.1061A>T	NP_112420.1:p.Gln354Leu
XM_005268826.1:c.1061A>T	XP_005268883.1:p.Gln354Leu
XR_245923.1:n.1173A>T
XR_245924.1:n.1017A>T
NM_002136.3:c.905A>T	NP_002127.1:p.Gln302Leu
NM_031157.3:c.1061A>T	NP_112420.1:p.Gln354Leu
NR_135167.1:n.1023A>T
XM_005268826.2:c.1061A>T	XP_005268883.1:p.Gln354Leu
XR_245923.2:n.1133A>T
NM_002136.4:c.905A>T	NP_002127.1:p.Gln302Leu
NM_031157.4:c.1061A>T MANE Select	NP_112420.1:p.Gln354Leu
NR_135167.2:n.987A>T