Canonical Allele Identifier: CA163083

Gene: HNRNPA1

Linked Data

• ClinVar Variation Id: 135608
• ClinVar RCV Id: RCV000122457
• dbSNP Id: rs483353038
• MyVariant Identifiers: chr12:g.54677746A>G (hg19) ; chr12:g.54283962A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.54283962A>G , CM000674.2:g.54283962A>G	GRCh38
NC_000012.11:g.54677746A>G , CM000674.1:g.54677746A>G	GRCh37
NC_000012.10:g.52964013A>G	NCBI36
NG_033830.1:g.8259A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340913.11:c.1058A>G MANE Select	ENSP00000341826.7:p.Asn353Ser
ENST00000550482.2:c.902A>G	ENSP00000446486.2:p.Asn301Ser
ENST00000676472.1:c.190A>G
ENST00000676572.1:c.284A>G
ENST00000676707.1:c.205A>G
ENST00000676725.1:n.1232A>G
ENST00000676794.1:c.77A>G	ENSP00000504819.1:p.Asn26Ser
ENST00000676853.1:c.286A>G
ENST00000676886.1:c.85-296A>G
ENST00000676951.1:c.307A>G
ENST00000677191.1:c.398A>G
ENST00000677210.1:c.1058A>G	ENSP00000503610.1:p.Asn353Ser
ENST00000677220.1:c.132+2460A>G	ENSP00000502987.1:n.132+2460A>G
ENST00000677224.1:c.160A>G
ENST00000677249.1:c.899A>G	ENSP00000503649.1:p.Asn300Ser
ENST00000677279.1:c.157A>G
ENST00000677375.1:c.902A>G	ENSP00000503651.1:p.Asn301Ser
ENST00000677385.1:c.*1244A>G	ENSP00000502985.1:n.*1244A>G
ENST00000677518.1:c.121A>G
ENST00000677539.1:c.440A>G
ENST00000677636.1:c.244A>G
ENST00000677778.1:c.75+1088A>G
ENST00000677840.1:c.151A>G
ENST00000677847.1:c.91A>G
ENST00000677945.1:c.229A>G
ENST00000678077.1:c.767A>G	ENSP00000504814.1:p.Asn256Ser
ENST00000678212.1:c.246A>G
ENST00000678279.1:n.137A>G
ENST00000678365.1:n.49-2700A>G
ENST00000678412.1:c.157-296A>G
ENST00000678418.1:n.1254A>G
ENST00000678424.1:c.283A>G
ENST00000678448.1:c.250A>G	ENSP00000503619.1:n.250A>G
ENST00000678456.1:c.76-296A>G
ENST00000678513.1:c.178A>G
ENST00000678581.1:c.286A>G
ENST00000678597.1:c.175A>G
ENST00000678611.1:c.292A>G
ENST00000678873.1:c.226A>G
ENST00000678876.1:c.244A>G
ENST00000678934.1:c.205A>G
ENST00000678970.1:c.227A>G
ENST00000679026.1:c.151A>G
ENST00000679063.1:c.226A>G
ENST00000679079.1:c.157-587A>G
ENST00000679228.1:n.1253A>G
ENST00000679273.1:c.238A>G	ENSP00000504626.1:n.238A>G
ENST00000679344.1:c.259A>G
ENST00000330752.12:c.863A>G	ENSP00000333504.8:p.Asn288Ser
ENST00000340913.10:c.1058A>G	ENSP00000341826.6:p.Asn353Ser
ENST00000546500.5:c.902A>G	ENSP00000448617.1:p.Asn301Ser
ENST00000547276.5:c.743A>G	ENSP00000447260.1:p.Asn248Ser
ENST00000547566.5:c.902A>G	ENSP00000449913.1:p.Asn301Ser
ENST00000550482.1:c.515A>G	ENSP00000446486.1:p.Asn172Ser
ENST00000551679.1:n.240A>G
NM_002136.2:c.902A>G	NP_002127.1:p.Asn301Ser
NM_031157.2:c.1058A>G	NP_112420.1:p.Asn353Ser
XM_005268826.1:c.1058A>G	XP_005268883.1:p.Asn353Ser
XR_245923.1:n.1170A>G
XR_245924.1:n.1014A>G
NM_002136.3:c.902A>G	NP_002127.1:p.Asn301Ser
NM_031157.3:c.1058A>G	NP_112420.1:p.Asn353Ser
NR_135167.1:n.1020A>G
XM_005268826.2:c.1058A>G	XP_005268883.1:p.Asn353Ser
XR_245923.2:n.1130A>G
NM_002136.4:c.902A>G	NP_002127.1:p.Asn301Ser
NM_031157.4:c.1058A>G MANE Select	NP_112420.1:p.Asn353Ser
NR_135167.2:n.984A>G