Canonical Allele Identifier: CA385122547

Gene: HNRNPA1

Linked Data

• MyVariant Identifiers: chr12:g.54677751G>T (hg19) ; chr12:g.54283967G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.54283967G>T , CM000674.2:g.54283967G>T	GRCh38
NC_000012.11:g.54677751G>T , CM000674.1:g.54677751G>T	GRCh37
NC_000012.10:g.52964018G>T	NCBI36
NG_033830.1:g.8264G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000340913.11:c.1063G>T MANE Select	ENSP00000341826.7:p.Gly355Cys
ENST00000550482.2:c.907G>T	ENSP00000446486.2:p.Gly303Cys
ENST00000676472.1:c.195G>T
ENST00000676572.1:c.289G>T
ENST00000676707.1:c.210G>T
ENST00000676725.1:n.1237G>T
ENST00000676794.1:c.82G>T	ENSP00000504819.1:p.Gly28Cys
ENST00000676853.1:c.291G>T
ENST00000676886.1:c.85-291G>T
ENST00000676951.1:c.312G>T
ENST00000677191.1:c.403G>T
ENST00000677210.1:c.1063G>T	ENSP00000503610.1:p.Gly355Cys
ENST00000677220.1:c.132+2465G>T	ENSP00000502987.1:n.132+2465G>T
ENST00000677224.1:c.165G>T
ENST00000677249.1:c.904G>T	ENSP00000503649.1:p.Gly302Cys
ENST00000677279.1:c.162G>T
ENST00000677375.1:c.907G>T	ENSP00000503651.1:p.Glu303Ter
ENST00000677385.1:c.*1249G>T	ENSP00000502985.1:n.*1249G>T
ENST00000677518.1:c.126G>T
ENST00000677539.1:c.445G>T
ENST00000677636.1:c.249G>T
ENST00000677778.1:c.75+1093G>T
ENST00000677840.1:c.156G>T
ENST00000677847.1:c.96G>T
ENST00000677945.1:c.234G>T
ENST00000678077.1:c.772G>T	ENSP00000504814.1:p.Gly258Cys
ENST00000678212.1:c.251G>T
ENST00000678279.1:n.142G>T
ENST00000678365.1:n.49-2695G>T
ENST00000678412.1:c.157-291G>T
ENST00000678418.1:n.1259G>T
ENST00000678424.1:c.288G>T
ENST00000678448.1:c.255G>T	ENSP00000503619.1:n.255G>T
ENST00000678456.1:c.76-291G>T
ENST00000678513.1:c.183G>T
ENST00000678581.1:c.291G>T
ENST00000678597.1:c.180G>T
ENST00000678611.1:c.297G>T
ENST00000678873.1:c.231G>T
ENST00000678876.1:c.249G>T
ENST00000678934.1:c.210G>T
ENST00000678970.1:c.232G>T
ENST00000679026.1:c.156G>T
ENST00000679063.1:c.231G>T
ENST00000679079.1:c.157-582G>T
ENST00000679228.1:n.1258G>T
ENST00000679273.1:c.243G>T	ENSP00000504626.1:n.243G>T
ENST00000679344.1:c.264G>T
ENST00000330752.12:c.868G>T	ENSP00000333504.8:p.Gly290Cys
ENST00000340913.10:c.1063G>T	ENSP00000341826.6:p.Gly355Cys
ENST00000546500.5:c.907G>T	ENSP00000448617.1:p.Gly303Cys
ENST00000547276.5:c.748G>T	ENSP00000447260.1:p.Gly250Cys
ENST00000547566.5:c.907G>T	ENSP00000449913.1:p.Gly303Cys
ENST00000550482.1:c.520G>T	ENSP00000446486.1:p.Gly174Cys
ENST00000551679.1:n.245G>T
NM_002136.2:c.907G>T	NP_002127.1:p.Gly303Cys
NM_031157.2:c.1063G>T	NP_112420.1:p.Gly355Cys
XM_005268826.1:c.1063G>T	XP_005268883.1:p.Gly355Cys
XR_245923.1:n.1175G>T
XR_245924.1:n.1019G>T
NM_002136.3:c.907G>T	NP_002127.1:p.Gly303Cys
NM_031157.3:c.1063G>T	NP_112420.1:p.Gly355Cys
NR_135167.1:n.1025G>T
XM_005268826.2:c.1063G>T	XP_005268883.1:p.Gly355Cys
XR_245923.2:n.1135G>T
NM_002136.4:c.907G>T	NP_002127.1:p.Gly303Cys
NM_031157.4:c.1063G>T MANE Select	NP_112420.1:p.Gly355Cys
NR_135167.2:n.989G>T