Canonical Allele Identifier: CA385122318

Gene: HNRNPA1

Linked Data

• MyVariant Identifiers: chr12:g.54677642C>A (hg19) ; chr12:g.54283858C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.54283858C>A , CM000674.2:g.54283858C>A	GRCh38
NC_000012.11:g.54677642C>A , CM000674.1:g.54677642C>A	GRCh37
NC_000012.10:g.52963909C>A	NCBI36
NG_033830.1:g.8155C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340913.11:c.954C>A MANE Select	ENSP00000341826.7:p.Tyr318Ter
ENST00000550482.2:c.798C>A	ENSP00000446486.2:p.Tyr266Ter
ENST00000676472.1:c.86C>A
ENST00000676572.1:c.180C>A
ENST00000676707.1:c.101C>A
ENST00000676725.1:n.1128C>A
ENST00000676794.1:c.-28C>A	ENSP00000504819.1:n.-28C>A
ENST00000676853.1:c.182C>A
ENST00000676886.1:c.85-400C>A
ENST00000676951.1:c.203C>A
ENST00000677191.1:c.294C>A
ENST00000677210.1:c.954C>A	ENSP00000503610.1:p.Tyr318Ter
ENST00000677220.1:c.132+2356C>A	ENSP00000502987.1:n.132+2356C>A
ENST00000677224.1:c.56C>A
ENST00000677249.1:c.795C>A	ENSP00000503649.1:p.Tyr265Ter
ENST00000677279.1:c.53C>A
ENST00000677375.1:c.798C>A	ENSP00000503651.1:p.Tyr266Ter
ENST00000677385.1:c.*1140C>A	ENSP00000502985.1:n.*1140C>A
ENST00000677518.1:c.47C>A
ENST00000677539.1:c.336C>A
ENST00000677636.1:c.140C>A
ENST00000677778.1:c.75+984C>A
ENST00000677840.1:c.47C>A
ENST00000677847.1:c.24+23C>A
ENST00000677945.1:c.125C>A
ENST00000678077.1:c.663C>A	ENSP00000504814.1:p.Tyr221Ter
ENST00000678212.1:c.142C>A
ENST00000678279.1:n.67-34C>A
ENST00000678365.1:n.49-2804C>A
ENST00000678412.1:c.157-400C>A
ENST00000678418.1:n.1150C>A
ENST00000678424.1:c.179C>A
ENST00000678448.1:c.146C>A	ENSP00000503619.1:p.Thr49Lys
ENST00000678456.1:c.76-400C>A
ENST00000678513.1:c.74C>A
ENST00000678581.1:c.182C>A
ENST00000678597.1:c.71C>A
ENST00000678611.1:c.188C>A
ENST00000678873.1:c.122C>A
ENST00000678876.1:c.140C>A
ENST00000678934.1:c.101C>A
ENST00000678970.1:c.157-34C>A
ENST00000679026.1:c.47C>A
ENST00000679063.1:c.122C>A
ENST00000679079.1:c.156+624C>A
ENST00000679228.1:n.1149C>A
ENST00000679273.1:c.134C>A	ENSP00000504626.1:p.Thr45Lys
ENST00000679344.1:c.155C>A
ENST00000330752.12:c.759C>A	ENSP00000333504.8:p.Tyr253Ter
ENST00000340913.10:c.954C>A	ENSP00000341826.6:p.Tyr318Ter
ENST00000546500.5:c.798C>A	ENSP00000448617.1:p.Tyr266Ter
ENST00000547276.5:c.639C>A	ENSP00000447260.1:p.Tyr213Ter
ENST00000547566.5:c.798C>A	ENSP00000449913.1:p.Tyr266Ter
ENST00000547708.5:c.450C>A	ENSP00000448229.1:p.Tyr150Ter
ENST00000550482.1:c.411C>A	ENSP00000446486.1:p.Tyr137Ter
ENST00000551679.1:n.136C>A
NM_002136.2:c.798C>A	NP_002127.1:p.Tyr266Ter
NM_031157.2:c.954C>A	NP_112420.1:p.Tyr318Ter
XM_005268826.1:c.954C>A	XP_005268883.1:p.Tyr318Ter
XR_245923.1:n.1066C>A
XR_245924.1:n.910C>A
NM_002136.3:c.798C>A	NP_002127.1:p.Tyr266Ter
NM_031157.3:c.954C>A	NP_112420.1:p.Tyr318Ter
NR_135167.1:n.916C>A
XM_005268826.2:c.954C>A	XP_005268883.1:p.Tyr318Ter
XR_245923.2:n.1026C>A
NM_002136.4:c.798C>A	NP_002127.1:p.Tyr266Ter
NM_031157.4:c.954C>A MANE Select	NP_112420.1:p.Tyr318Ter
NR_135167.2:n.880C>A