Canonical Allele Identifier: CA385122298

Gene: HNRNPA1

Linked Data

• MyVariant Identifiers: chr12:g.54677633T>A (hg19) ; chr12:g.54283849T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.54283849T>A , CM000674.2:g.54283849T>A	GRCh38
NC_000012.11:g.54677633T>A , CM000674.1:g.54677633T>A	GRCh37
NC_000012.10:g.52963900T>A	NCBI36
NG_033830.1:g.8146T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000340913.11:c.945T>A MANE Select	ENSP00000341826.7:p.Phe315Leu
ENST00000550482.2:c.789T>A	ENSP00000446486.2:p.Phe263Leu
ENST00000676472.1:c.77T>A
ENST00000676572.1:c.171T>A
ENST00000676707.1:c.92T>A
ENST00000676725.1:n.1119T>A
ENST00000676794.1:c.-37T>A	ENSP00000504819.1:n.-37T>A
ENST00000676853.1:c.173T>A
ENST00000676886.1:c.85-409T>A
ENST00000676951.1:c.194T>A
ENST00000677191.1:c.285T>A
ENST00000677210.1:c.945T>A	ENSP00000503610.1:p.Phe315Leu
ENST00000677220.1:c.132+2347T>A	ENSP00000502987.1:n.132+2347T>A
ENST00000677224.1:c.47T>A
ENST00000677249.1:c.786T>A	ENSP00000503649.1:p.Phe262Leu
ENST00000677279.1:c.44T>A
ENST00000677375.1:c.789T>A	ENSP00000503651.1:p.Phe263Leu
ENST00000677385.1:c.*1131T>A	ENSP00000502985.1:n.*1131T>A
ENST00000677518.1:c.38T>A
ENST00000677539.1:c.327T>A
ENST00000677636.1:c.131T>A
ENST00000677778.1:c.75+975T>A
ENST00000677840.1:c.38T>A
ENST00000677847.1:c.24+14T>A
ENST00000677945.1:c.116T>A
ENST00000678077.1:c.654T>A	ENSP00000504814.1:p.Phe218Leu
ENST00000678212.1:c.133T>A
ENST00000678279.1:n.67-43T>A
ENST00000678365.1:n.49-2813T>A
ENST00000678412.1:c.157-409T>A
ENST00000678418.1:n.1141T>A
ENST00000678424.1:c.170T>A
ENST00000678448.1:c.137T>A	ENSP00000503619.1:p.Leu46Ter
ENST00000678456.1:c.76-409T>A
ENST00000678513.1:c.65T>A
ENST00000678581.1:c.173T>A
ENST00000678597.1:c.62T>A
ENST00000678611.1:c.179T>A
ENST00000678873.1:c.113T>A
ENST00000678876.1:c.131T>A
ENST00000678934.1:c.92T>A
ENST00000678970.1:c.157-43T>A
ENST00000679026.1:c.38T>A
ENST00000679063.1:c.113T>A
ENST00000679079.1:c.156+615T>A
ENST00000679228.1:n.1140T>A
ENST00000679273.1:c.125T>A	ENSP00000504626.1:p.Leu42Ter
ENST00000679344.1:c.146T>A
ENST00000330752.12:c.750T>A	ENSP00000333504.8:p.Phe250Leu
ENST00000340913.10:c.945T>A	ENSP00000341826.6:p.Phe315Leu
ENST00000546500.5:c.789T>A	ENSP00000448617.1:p.Phe263Leu
ENST00000547276.5:c.630T>A	ENSP00000447260.1:p.Phe210Leu
ENST00000547566.5:c.789T>A	ENSP00000449913.1:p.Phe263Leu
ENST00000547708.5:c.441T>A	ENSP00000448229.1:p.Phe147Leu
ENST00000550482.1:c.402T>A	ENSP00000446486.1:p.Phe134Leu
ENST00000551679.1:n.127T>A
NM_002136.2:c.789T>A	NP_002127.1:p.Phe263Leu
NM_031157.2:c.945T>A	NP_112420.1:p.Phe315Leu
XM_005268826.1:c.945T>A	XP_005268883.1:p.Phe315Leu
XR_245923.1:n.1057T>A
XR_245924.1:n.901T>A
NM_002136.3:c.789T>A	NP_002127.1:p.Phe263Leu
NM_031157.3:c.945T>A	NP_112420.1:p.Phe315Leu
NR_135167.1:n.907T>A
XM_005268826.2:c.945T>A	XP_005268883.1:p.Phe315Leu
XR_245923.2:n.1017T>A
NM_002136.4:c.789T>A	NP_002127.1:p.Phe263Leu
NM_031157.4:c.945T>A MANE Select	NP_112420.1:p.Phe315Leu
NR_135167.2:n.871T>A