Canonical Allele Identifier: CA163053

Gene: HNRNPA1

Linked Data

• ClinVar Variation Id: 135598
• ClinVar RCV Id: RCV000122447
• dbSNP Id: rs483353030
• MyVariant Identifiers: chr12:g.54677675G>T (hg19) ; chr12:g.54283891G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.54283891G>T , CM000674.2:g.54283891G>T	GRCh38
NC_000012.11:g.54677675G>T , CM000674.1:g.54677675G>T	GRCh37
NC_000012.10:g.52963942G>T	NCBI36
NG_033830.1:g.8188G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340913.11:c.987G>T MANE Select	ENSP00000341826.7:p.Lys329Asn
ENST00000550482.2:c.831G>T	ENSP00000446486.2:p.Lys277Asn
ENST00000676472.1:c.119G>T
ENST00000676572.1:c.213G>T
ENST00000676707.1:c.134G>T
ENST00000676725.1:n.1161G>T
ENST00000676794.1:c.6G>T	ENSP00000504819.1:p.Lys2Asn
ENST00000676853.1:c.215G>T
ENST00000676886.1:c.85-367G>T
ENST00000676951.1:c.236G>T
ENST00000677191.1:c.327G>T
ENST00000677210.1:c.987G>T	ENSP00000503610.1:p.Lys329Asn
ENST00000677220.1:c.132+2389G>T	ENSP00000502987.1:n.132+2389G>T
ENST00000677224.1:c.89G>T
ENST00000677249.1:c.828G>T	ENSP00000503649.1:p.Lys276Asn
ENST00000677279.1:c.86G>T
ENST00000677375.1:c.831G>T	ENSP00000503651.1:p.Lys277Asn
ENST00000677385.1:c.*1173G>T	ENSP00000502985.1:n.*1173G>T
ENST00000677518.1:c.80G>T
ENST00000677539.1:c.369G>T
ENST00000677636.1:c.173G>T
ENST00000677778.1:c.75+1017G>T
ENST00000677840.1:c.80G>T
ENST00000677847.1:c.25-5G>T
ENST00000677945.1:c.158G>T
ENST00000678077.1:c.696G>T	ENSP00000504814.1:p.Lys232Asn
ENST00000678212.1:c.175G>T
ENST00000678279.1:n.67-1G>T
ENST00000678365.1:n.49-2771G>T
ENST00000678412.1:c.157-367G>T
ENST00000678418.1:n.1183G>T
ENST00000678424.1:c.212G>T
ENST00000678448.1:c.179G>T	ENSP00000503619.1:n.179G>T
ENST00000678456.1:c.76-367G>T
ENST00000678513.1:c.107G>T
ENST00000678581.1:c.215G>T
ENST00000678597.1:c.104G>T
ENST00000678611.1:c.221G>T
ENST00000678873.1:c.155G>T
ENST00000678876.1:c.173G>T
ENST00000678934.1:c.134G>T
ENST00000678970.1:c.157-1G>T
ENST00000679026.1:c.80G>T
ENST00000679063.1:c.155G>T
ENST00000679079.1:c.157-658G>T
ENST00000679228.1:n.1182G>T
ENST00000679273.1:c.167G>T	ENSP00000504626.1:n.167G>T
ENST00000679344.1:c.188G>T
ENST00000330752.12:c.792G>T	ENSP00000333504.8:p.Lys264Asn
ENST00000340913.10:c.987G>T	ENSP00000341826.6:p.Lys329Asn
ENST00000546500.5:c.831G>T	ENSP00000448617.1:p.Lys277Asn
ENST00000547276.5:c.672G>T	ENSP00000447260.1:p.Lys224Asn
ENST00000547566.5:c.831G>T	ENSP00000449913.1:p.Lys277Asn
ENST00000550482.1:c.444G>T	ENSP00000446486.1:p.Lys148Asn
ENST00000551679.1:n.169G>T
NM_002136.2:c.831G>T	NP_002127.1:p.Lys277Asn
NM_031157.2:c.987G>T	NP_112420.1:p.Lys329Asn
XM_005268826.1:c.987G>T	XP_005268883.1:p.Lys329Asn
XR_245923.1:n.1099G>T
XR_245924.1:n.943G>T
NM_002136.3:c.831G>T	NP_002127.1:p.Lys277Asn
NM_031157.3:c.987G>T	NP_112420.1:p.Lys329Asn
NR_135167.1:n.949G>T
XM_005268826.2:c.987G>T	XP_005268883.1:p.Lys329Asn
XR_245923.2:n.1059G>T
NM_002136.4:c.831G>T	NP_002127.1:p.Lys277Asn
NM_031157.4:c.987G>T MANE Select	NP_112420.1:p.Lys329Asn
NR_135167.2:n.913G>T