Canonical Allele Identifier: CA385122550

Gene: HNRNPA1

Linked Data

• MyVariant Identifiers: chr12:g.54677752G>C (hg19) ; chr12:g.54283968G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.54283968G>C , CM000674.2:g.54283968G>C	GRCh38
NC_000012.11:g.54677752G>C , CM000674.1:g.54677752G>C	GRCh37
NC_000012.10:g.52964019G>C	NCBI36
NG_033830.1:g.8265G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340913.11:c.1063+1G>C MANE Select	ENSP00000341826.7:n.1063+1G>C
ENST00000550482.2:c.907+1G>C	ENSP00000446486.2:n.907+1G>C
ENST00000676572.1:c.289+1G>C
ENST00000676725.1:n.1237+1G>C
ENST00000676794.1:c.82+1G>C	ENSP00000504819.1:n.82+1G>C
ENST00000676886.1:c.85-290G>C
ENST00000677191.1:c.403+1G>C
ENST00000677210.1:c.1063+1G>C	ENSP00000503610.1:n.1063+1G>C
ENST00000677220.1:c.132+2466G>C	ENSP00000502987.1:n.132+2466G>C
ENST00000677249.1:c.904+1G>C	ENSP00000503649.1:n.904+1G>C
ENST00000677375.1:c.907+1G>C	ENSP00000503651.1:n.907+1G>C
ENST00000677385.1:c.*1250G>C	ENSP00000502985.1:n.*1250G>C
ENST00000677778.1:c.75+1094G>C
ENST00000677840.1:c.156+1G>C
ENST00000678077.1:c.772+1G>C	ENSP00000504814.1:n.772+1G>C
ENST00000678212.1:c.251+1G>C
ENST00000678365.1:n.49-2694G>C
ENST00000678412.1:c.157-290G>C
ENST00000678418.1:n.1259+1G>C
ENST00000678448.1:c.255+1G>C	ENSP00000503619.1:n.255+1G>C
ENST00000678456.1:c.76-290G>C
ENST00000678970.1:c.232+1G>C
ENST00000679026.1:c.156+1G>C
ENST00000679079.1:c.157-581G>C
ENST00000679228.1:n.1258+1G>C
ENST00000679273.1:c.243+1G>C	ENSP00000504626.1:n.243+1G>C
ENST00000679344.1:c.264+1G>C
ENST00000330752.12:c.868+1G>C	ENSP00000333504.8:n.868+1G>C
ENST00000340913.10:c.1063+1G>C	ENSP00000341826.6:n.1063+1G>C
ENST00000546500.5:c.907+1G>C	ENSP00000448617.1:n.907+1G>C
ENST00000547276.5:c.748+1G>C	ENSP00000447260.1:n.748+1G>C
ENST00000547566.5:c.907+1G>C	ENSP00000449913.1:n.907+1G>C
ENST00000550482.1:c.520+1G>C	ENSP00000446486.1:n.520+1G>C
ENST00000551679.1:n.245+1G>C
NM_002136.2:c.907+1G>C	NP_002127.1:n.907+1G>C
NM_031157.2:c.1063+1G>C	NP_112420.1:n.1063+1G>C
XM_005268826.1:c.1063+1G>C	XP_005268883.1:n.1063+1G>C
XR_245923.1:n.1175+1G>C
XR_245924.1:n.1019+1G>C
NM_002136.3:c.907+1G>C	NP_002127.1:n.907+1G>C
NM_031157.3:c.1063+1G>C	NP_112420.1:n.1063+1G>C
NR_135167.1:n.1025+1G>C
XM_005268826.2:c.1063+1G>C	XP_005268883.1:n.1063+1G>C
XR_245923.2:n.1135+1G>C
NM_002136.4:c.907+1G>C	NP_002127.1:n.907+1G>C
NM_031157.4:c.1063+1G>C MANE Select	NP_112420.1:n.1063+1G>C
NR_135167.2:n.989+1G>C