Canonical Allele Identifier: CA385122536

Gene: HNRNPA1

Linked Data

• MyVariant Identifiers: chr12:g.54677747C>A (hg19) ; chr12:g.54283963C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.54283963C>A , CM000674.2:g.54283963C>A	GRCh38
NC_000012.11:g.54677747C>A , CM000674.1:g.54677747C>A	GRCh37
NC_000012.10:g.52964014C>A	NCBI36
NG_033830.1:g.8260C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340913.11:c.1059C>A MANE Select	ENSP00000341826.7:p.Asn353Lys
ENST00000550482.2:c.903C>A	ENSP00000446486.2:p.Asn301Lys
ENST00000676472.1:c.191C>A
ENST00000676572.1:c.285C>A
ENST00000676707.1:c.206C>A
ENST00000676725.1:n.1233C>A
ENST00000676794.1:c.78C>A	ENSP00000504819.1:p.Asn26Lys
ENST00000676853.1:c.287C>A
ENST00000676886.1:c.85-295C>A
ENST00000676951.1:c.308C>A
ENST00000677191.1:c.399C>A
ENST00000677210.1:c.1059C>A	ENSP00000503610.1:p.Asn353Lys
ENST00000677220.1:c.132+2461C>A	ENSP00000502987.1:n.132+2461C>A
ENST00000677224.1:c.161C>A
ENST00000677249.1:c.900C>A	ENSP00000503649.1:p.Asn300Lys
ENST00000677279.1:c.158C>A
ENST00000677375.1:c.903C>A	ENSP00000503651.1:p.Asn301Lys
ENST00000677385.1:c.*1245C>A	ENSP00000502985.1:n.*1245C>A
ENST00000677518.1:c.122C>A
ENST00000677539.1:c.441C>A
ENST00000677636.1:c.245C>A
ENST00000677778.1:c.75+1089C>A
ENST00000677840.1:c.152C>A
ENST00000677847.1:c.92C>A
ENST00000677945.1:c.230C>A
ENST00000678077.1:c.768C>A	ENSP00000504814.1:p.Asn256Lys
ENST00000678212.1:c.247C>A
ENST00000678279.1:n.138C>A
ENST00000678365.1:n.49-2699C>A
ENST00000678412.1:c.157-295C>A
ENST00000678418.1:n.1255C>A
ENST00000678424.1:c.284C>A
ENST00000678448.1:c.251C>A	ENSP00000503619.1:n.251C>A
ENST00000678456.1:c.76-295C>A
ENST00000678513.1:c.179C>A
ENST00000678581.1:c.287C>A
ENST00000678597.1:c.176C>A
ENST00000678611.1:c.293C>A
ENST00000678873.1:c.227C>A
ENST00000678876.1:c.245C>A
ENST00000678934.1:c.206C>A
ENST00000678970.1:c.228C>A
ENST00000679026.1:c.152C>A
ENST00000679063.1:c.227C>A
ENST00000679079.1:c.157-586C>A
ENST00000679228.1:n.1254C>A
ENST00000679273.1:c.239C>A	ENSP00000504626.1:n.239C>A
ENST00000679344.1:c.260C>A
ENST00000330752.12:c.864C>A	ENSP00000333504.8:p.Asn288Lys
ENST00000340913.10:c.1059C>A	ENSP00000341826.6:p.Asn353Lys
ENST00000546500.5:c.903C>A	ENSP00000448617.1:p.Asn301Lys
ENST00000547276.5:c.744C>A	ENSP00000447260.1:p.Asn248Lys
ENST00000547566.5:c.903C>A	ENSP00000449913.1:p.Asn301Lys
ENST00000550482.1:c.516C>A	ENSP00000446486.1:p.Asn172Lys
ENST00000551679.1:n.241C>A
NM_002136.2:c.903C>A	NP_002127.1:p.Asn301Lys
NM_031157.2:c.1059C>A	NP_112420.1:p.Asn353Lys
XM_005268826.1:c.1059C>A	XP_005268883.1:p.Asn353Lys
XR_245923.1:n.1171C>A
XR_245924.1:n.1015C>A
NM_002136.3:c.903C>A	NP_002127.1:p.Asn301Lys
NM_031157.3:c.1059C>A	NP_112420.1:p.Asn353Lys
NR_135167.1:n.1021C>A
XM_005268826.2:c.1059C>A	XP_005268883.1:p.Asn353Lys
XR_245923.2:n.1131C>A
NM_002136.4:c.903C>A	NP_002127.1:p.Asn301Lys
NM_031157.4:c.1059C>A MANE Select	NP_112420.1:p.Asn353Lys
NR_135167.2:n.985C>A