Canonical Allele Identifier: CA480005680

Gene: HNRNPA1

Linked Data

• MyVariant Identifiers: chr12:g.54677636G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.54283852G>A , CM000674.2:g.54283852G>A	GRCh38
NC_000012.11:g.54677636G>A , CM000674.1:g.54677636G>A	GRCh37
NC_000012.10:g.52963903G>A	NCBI36
NG_033830.1:g.8149G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000340913.11:c.948G>A MANE Select	ENSP00000341826.7:p.Gly316=
ENST00000550482.2:c.792G>A	ENSP00000446486.2:p.Gly264=
ENST00000676472.1:c.80G>A
ENST00000676572.1:c.174G>A
ENST00000676707.1:c.95G>A
ENST00000676725.1:n.1122G>A
ENST00000676794.1:c.-34G>A	ENSP00000504819.1:n.-34G>A
ENST00000676853.1:c.176G>A
ENST00000676886.1:c.85-406G>A
ENST00000676951.1:c.197G>A
ENST00000677191.1:c.288G>A
ENST00000677210.1:c.948G>A	ENSP00000503610.1:p.Gly316=
ENST00000677220.1:c.132+2350G>A	ENSP00000502987.1:n.132+2350G>A
ENST00000677224.1:c.50G>A
ENST00000677249.1:c.789G>A	ENSP00000503649.1:p.Gly263=
ENST00000677279.1:c.47G>A
ENST00000677375.1:c.792G>A	ENSP00000503651.1:p.Gly264=
ENST00000677385.1:c.*1134G>A	ENSP00000502985.1:n.*1134G>A
ENST00000677518.1:c.41G>A
ENST00000677539.1:c.330G>A
ENST00000677636.1:c.134G>A
ENST00000677778.1:c.75+978G>A
ENST00000677840.1:c.41G>A
ENST00000677847.1:c.24+17G>A
ENST00000677945.1:c.119G>A
ENST00000678077.1:c.657G>A	ENSP00000504814.1:p.Gly219=
ENST00000678212.1:c.136G>A
ENST00000678279.1:n.67-40G>A
ENST00000678365.1:n.49-2810G>A
ENST00000678412.1:c.157-406G>A
ENST00000678418.1:n.1144G>A
ENST00000678424.1:c.173G>A
ENST00000678448.1:c.140G>A	ENSP00000503619.1:p.Gly47Glu
ENST00000678456.1:c.76-406G>A
ENST00000678513.1:c.68G>A
ENST00000678581.1:c.176G>A
ENST00000678597.1:c.65G>A
ENST00000678611.1:c.182G>A
ENST00000678873.1:c.116G>A
ENST00000678876.1:c.134G>A
ENST00000678934.1:c.95G>A
ENST00000678970.1:c.157-40G>A
ENST00000679026.1:c.41G>A
ENST00000679063.1:c.116G>A
ENST00000679079.1:c.156+618G>A
ENST00000679228.1:n.1143G>A
ENST00000679273.1:c.128G>A	ENSP00000504626.1:p.Gly43Glu
ENST00000679344.1:c.149G>A
ENST00000330752.12:c.753G>A	ENSP00000333504.8:p.Gly251=
ENST00000340913.10:c.948G>A	ENSP00000341826.6:p.Gly316=
ENST00000546500.5:c.792G>A	ENSP00000448617.1:p.Gly264=
ENST00000547276.5:c.633G>A	ENSP00000447260.1:p.Gly211=
ENST00000547566.5:c.792G>A	ENSP00000449913.1:p.Gly264=
ENST00000547708.5:c.444G>A	ENSP00000448229.1:p.Gly148=
ENST00000550482.1:c.405G>A	ENSP00000446486.1:p.Gly135=
ENST00000551679.1:n.130G>A
NM_002136.2:c.792G>A	NP_002127.1:p.Gly264=
NM_031157.2:c.948G>A	NP_112420.1:p.Gly316=
XM_005268826.1:c.948G>A	XP_005268883.1:p.Gly316=
XR_245923.1:n.1060G>A
XR_245924.1:n.904G>A
NM_002136.3:c.792G>A	NP_002127.1:p.Gly264=
NM_031157.3:c.948G>A	NP_112420.1:p.Gly316=
NR_135167.1:n.910G>A
XM_005268826.2:c.948G>A	XP_005268883.1:p.Gly316=
XR_245923.2:n.1020G>A
NM_002136.4:c.792G>A	NP_002127.1:p.Gly264=
NM_031157.4:c.948G>A MANE Select	NP_112420.1:p.Gly316=
NR_135167.2:n.874G>A