Canonical Allele Identifier: CA385122308

Gene: HNRNPA1

Linked Data

• MyVariant Identifiers: chr12:g.54677638A>T (hg19) ; chr12:g.54283854A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.54283854A>T , CM000674.2:g.54283854A>T	GRCh38
NC_000012.11:g.54677638A>T , CM000674.1:g.54677638A>T	GRCh37
NC_000012.10:g.52963905A>T	NCBI36
NG_033830.1:g.8151A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000340913.11:c.950A>T MANE Select	ENSP00000341826.7:p.Asn317Ile
ENST00000550482.2:c.794A>T	ENSP00000446486.2:p.Asn265Ile
ENST00000676472.1:c.82A>T
ENST00000676572.1:c.176A>T
ENST00000676707.1:c.97A>T
ENST00000676725.1:n.1124A>T
ENST00000676794.1:c.-32A>T	ENSP00000504819.1:n.-32A>T
ENST00000676853.1:c.178A>T
ENST00000676886.1:c.85-404A>T
ENST00000676951.1:c.199A>T
ENST00000677191.1:c.290A>T
ENST00000677210.1:c.950A>T	ENSP00000503610.1:p.Asn317Ile
ENST00000677220.1:c.132+2352A>T	ENSP00000502987.1:n.132+2352A>T
ENST00000677224.1:c.52A>T
ENST00000677249.1:c.791A>T	ENSP00000503649.1:p.Asn264Ile
ENST00000677279.1:c.49A>T
ENST00000677375.1:c.794A>T	ENSP00000503651.1:p.Asn265Ile
ENST00000677385.1:c.*1136A>T	ENSP00000502985.1:n.*1136A>T
ENST00000677518.1:c.43A>T
ENST00000677539.1:c.332A>T
ENST00000677636.1:c.136A>T
ENST00000677778.1:c.75+980A>T
ENST00000677840.1:c.43A>T
ENST00000677847.1:c.24+19A>T
ENST00000677945.1:c.121A>T
ENST00000678077.1:c.659A>T	ENSP00000504814.1:p.Asn220Ile
ENST00000678212.1:c.138A>T
ENST00000678279.1:n.67-38A>T
ENST00000678365.1:n.49-2808A>T
ENST00000678412.1:c.157-404A>T
ENST00000678418.1:n.1146A>T
ENST00000678424.1:c.175A>T
ENST00000678448.1:c.142A>T	ENSP00000503619.1:p.Ile48Phe
ENST00000678456.1:c.76-404A>T
ENST00000678513.1:c.70A>T
ENST00000678581.1:c.178A>T
ENST00000678597.1:c.67A>T
ENST00000678611.1:c.184A>T
ENST00000678873.1:c.118A>T
ENST00000678876.1:c.136A>T
ENST00000678934.1:c.97A>T
ENST00000678970.1:c.157-38A>T
ENST00000679026.1:c.43A>T
ENST00000679063.1:c.118A>T
ENST00000679079.1:c.156+620A>T
ENST00000679228.1:n.1145A>T
ENST00000679273.1:c.130A>T	ENSP00000504626.1:p.Ile44Phe
ENST00000679344.1:c.151A>T
ENST00000330752.12:c.755A>T	ENSP00000333504.8:p.Asn252Ile
ENST00000340913.10:c.950A>T	ENSP00000341826.6:p.Asn317Ile
ENST00000546500.5:c.794A>T	ENSP00000448617.1:p.Asn265Ile
ENST00000547276.5:c.635A>T	ENSP00000447260.1:p.Asn212Ile
ENST00000547566.5:c.794A>T	ENSP00000449913.1:p.Asn265Ile
ENST00000547708.5:c.446A>T	ENSP00000448229.1:p.Asn149Ile
ENST00000550482.1:c.407A>T	ENSP00000446486.1:p.Asn136Ile
ENST00000551679.1:n.132A>T
NM_002136.2:c.794A>T	NP_002127.1:p.Asn265Ile
NM_031157.2:c.950A>T	NP_112420.1:p.Asn317Ile
XM_005268826.1:c.950A>T	XP_005268883.1:p.Asn317Ile
XR_245923.1:n.1062A>T
XR_245924.1:n.906A>T
NM_002136.3:c.794A>T	NP_002127.1:p.Asn265Ile
NM_031157.3:c.950A>T	NP_112420.1:p.Asn317Ile
NR_135167.1:n.912A>T
XM_005268826.2:c.950A>T	XP_005268883.1:p.Asn317Ile
XR_245923.2:n.1022A>T
NM_002136.4:c.794A>T	NP_002127.1:p.Asn265Ile
NM_031157.4:c.950A>T MANE Select	NP_112420.1:p.Asn317Ile
NR_135167.2:n.876A>T