Canonical Allele Identifier: CA385122301

Gene: HNRNPA1

Linked Data

• MyVariant Identifiers: chr12:g.54677634G>C (hg19) ; chr12:g.54283850G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.54283850G>C , CM000674.2:g.54283850G>C	GRCh38
NC_000012.11:g.54677634G>C , CM000674.1:g.54677634G>C	GRCh37
NC_000012.10:g.52963901G>C	NCBI36
NG_033830.1:g.8147G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000340913.11:c.946G>C MANE Select	ENSP00000341826.7:p.Gly316Arg
ENST00000550482.2:c.790G>C	ENSP00000446486.2:p.Gly264Arg
ENST00000676472.1:c.78G>C
ENST00000676572.1:c.172G>C
ENST00000676707.1:c.93G>C
ENST00000676725.1:n.1120G>C
ENST00000676794.1:c.-36G>C	ENSP00000504819.1:n.-36G>C
ENST00000676853.1:c.174G>C
ENST00000676886.1:c.85-408G>C
ENST00000676951.1:c.195G>C
ENST00000677191.1:c.286G>C
ENST00000677210.1:c.946G>C	ENSP00000503610.1:p.Gly316Arg
ENST00000677220.1:c.132+2348G>C	ENSP00000502987.1:n.132+2348G>C
ENST00000677224.1:c.48G>C
ENST00000677249.1:c.787G>C	ENSP00000503649.1:p.Gly263Arg
ENST00000677279.1:c.45G>C
ENST00000677375.1:c.790G>C	ENSP00000503651.1:p.Gly264Arg
ENST00000677385.1:c.*1132G>C	ENSP00000502985.1:n.*1132G>C
ENST00000677518.1:c.39G>C
ENST00000677539.1:c.328G>C
ENST00000677636.1:c.132G>C
ENST00000677778.1:c.75+976G>C
ENST00000677840.1:c.39G>C
ENST00000677847.1:c.24+15G>C
ENST00000677945.1:c.117G>C
ENST00000678077.1:c.655G>C	ENSP00000504814.1:p.Gly219Arg
ENST00000678212.1:c.134G>C
ENST00000678279.1:n.67-42G>C
ENST00000678365.1:n.49-2812G>C
ENST00000678412.1:c.157-408G>C
ENST00000678418.1:n.1142G>C
ENST00000678424.1:c.171G>C
ENST00000678448.1:c.138G>C	ENSP00000503619.1:p.Leu46Phe
ENST00000678456.1:c.76-408G>C
ENST00000678513.1:c.66G>C
ENST00000678581.1:c.174G>C
ENST00000678597.1:c.63G>C
ENST00000678611.1:c.180G>C
ENST00000678873.1:c.114G>C
ENST00000678876.1:c.132G>C
ENST00000678934.1:c.93G>C
ENST00000678970.1:c.157-42G>C
ENST00000679026.1:c.39G>C
ENST00000679063.1:c.114G>C
ENST00000679079.1:c.156+616G>C
ENST00000679228.1:n.1141G>C
ENST00000679273.1:c.126G>C	ENSP00000504626.1:p.Leu42Phe
ENST00000679344.1:c.147G>C
ENST00000330752.12:c.751G>C	ENSP00000333504.8:p.Gly251Arg
ENST00000340913.10:c.946G>C	ENSP00000341826.6:p.Gly316Arg
ENST00000546500.5:c.790G>C	ENSP00000448617.1:p.Gly264Arg
ENST00000547276.5:c.631G>C	ENSP00000447260.1:p.Gly211Arg
ENST00000547566.5:c.790G>C	ENSP00000449913.1:p.Gly264Arg
ENST00000547708.5:c.442G>C	ENSP00000448229.1:p.Gly148Arg
ENST00000550482.1:c.403G>C	ENSP00000446486.1:p.Gly135Arg
ENST00000551679.1:n.128G>C
NM_002136.2:c.790G>C	NP_002127.1:p.Gly264Arg
NM_031157.2:c.946G>C	NP_112420.1:p.Gly316Arg
XM_005268826.1:c.946G>C	XP_005268883.1:p.Gly316Arg
XR_245923.1:n.1058G>C
XR_245924.1:n.902G>C
NM_002136.3:c.790G>C	NP_002127.1:p.Gly264Arg
NM_031157.3:c.946G>C	NP_112420.1:p.Gly316Arg
NR_135167.1:n.908G>C
XM_005268826.2:c.946G>C	XP_005268883.1:p.Gly316Arg
XR_245923.2:n.1018G>C
NM_002136.4:c.790G>C	NP_002127.1:p.Gly264Arg
NM_031157.4:c.946G>C MANE Select	NP_112420.1:p.Gly316Arg
NR_135167.2:n.872G>C