Canonical Allele Identifier: CA6606399

Gene: HNRNPA1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.54283910A>C , CM000674.2:g.54283910A>C	GRCh38
NC_000012.11:g.54677694A>C , CM000674.1:g.54677694A>C	GRCh37
NC_000012.10:g.52963961A>C	NCBI36
NG_033830.1:g.8207A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340913.11:c.1006A>C MANE Select	ENSP00000341826.7:p.Arg336=
ENST00000550482.2:c.850A>C	ENSP00000446486.2:p.Arg284=
ENST00000676472.1:c.138A>C
ENST00000676572.1:c.232A>C
ENST00000676707.1:c.153A>C
ENST00000676725.1:n.1180A>C
ENST00000676794.1:c.25A>C	ENSP00000504819.1:p.Arg9=
ENST00000676853.1:c.234A>C
ENST00000676886.1:c.85-348A>C
ENST00000676951.1:c.255A>C
ENST00000677191.1:c.346A>C
ENST00000677210.1:c.1006A>C	ENSP00000503610.1:p.Arg336=
ENST00000677220.1:c.132+2408A>C	ENSP00000502987.1:n.132+2408A>C
ENST00000677224.1:c.108A>C
ENST00000677249.1:c.847A>C	ENSP00000503649.1:p.Arg283=
ENST00000677279.1:c.105A>C
ENST00000677375.1:c.850A>C	ENSP00000503651.1:p.Arg284=
ENST00000677385.1:c.*1192A>C	ENSP00000502985.1:n.*1192A>C
ENST00000677518.1:c.96+3A>C
ENST00000677539.1:c.388A>C
ENST00000677636.1:c.192A>C
ENST00000677778.1:c.75+1036A>C
ENST00000677840.1:c.99A>C
ENST00000677847.1:c.39A>C
ENST00000677945.1:c.177A>C
ENST00000678077.1:c.715A>C	ENSP00000504814.1:p.Arg239=
ENST00000678212.1:c.194A>C
ENST00000678279.1:n.85A>C
ENST00000678365.1:n.49-2752A>C
ENST00000678412.1:c.157-348A>C
ENST00000678418.1:n.1202A>C
ENST00000678424.1:c.231A>C
ENST00000678448.1:c.198A>C	ENSP00000503619.1:n.198A>C
ENST00000678456.1:c.76-348A>C
ENST00000678513.1:c.126A>C
ENST00000678581.1:c.234A>C
ENST00000678597.1:c.123A>C
ENST00000678611.1:c.240A>C
ENST00000678873.1:c.174A>C
ENST00000678876.1:c.192A>C
ENST00000678934.1:c.153A>C
ENST00000678970.1:c.175A>C
ENST00000679026.1:c.99A>C
ENST00000679063.1:c.174A>C
ENST00000679079.1:c.157-639A>C
ENST00000679228.1:n.1201A>C
ENST00000679273.1:c.186A>C	ENSP00000504626.1:n.186A>C
ENST00000679344.1:c.207A>C
ENST00000330752.12:c.811A>C	ENSP00000333504.8:p.Arg271=
ENST00000340913.10:c.1006A>C	ENSP00000341826.6:p.Arg336=
ENST00000546500.5:c.850A>C	ENSP00000448617.1:p.Arg284=
ENST00000547276.5:c.691A>C	ENSP00000447260.1:p.Arg231=
ENST00000547566.5:c.850A>C	ENSP00000449913.1:p.Arg284=
ENST00000550482.1:c.463A>C	ENSP00000446486.1:p.Arg155=
ENST00000551679.1:n.188A>C
NM_002136.2:c.850A>C	NP_002127.1:p.Arg284=
NM_031157.2:c.1006A>C	NP_112420.1:p.Arg336=
XM_005268826.1:c.1006A>C	XP_005268883.1:p.Arg336=
XR_245923.1:n.1118A>C
XR_245924.1:n.962A>C
NM_002136.3:c.850A>C	NP_002127.1:p.Arg284=
NM_031157.3:c.1006A>C	NP_112420.1:p.Arg336=
NR_135167.1:n.968A>C
XM_005268826.2:c.1006A>C	XP_005268883.1:p.Arg336=
XR_245923.2:n.1078A>C
NM_002136.4:c.850A>C	NP_002127.1:p.Arg284=
NM_031157.4:c.1006A>C MANE Select	NP_112420.1:p.Arg336=
NR_135167.2:n.932A>C