Canonical Allele Identifier: CA385122554

Gene: HNRNPA1

Linked Data

• MyVariant Identifiers: chr12:g.54677753T>G (hg19) ; chr12:g.54283969T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.54283969T>G , CM000674.2:g.54283969T>G	GRCh38
NC_000012.11:g.54677753T>G , CM000674.1:g.54677753T>G	GRCh37
NC_000012.10:g.52964020T>G	NCBI36
NG_033830.1:g.8266T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000340913.11:c.1063+2T>G MANE Select	ENSP00000341826.7:n.1063+2T>G
ENST00000550482.2:c.907+2T>G	ENSP00000446486.2:n.907+2T>G
ENST00000676572.1:c.289+2T>G
ENST00000676725.1:n.1237+2T>G
ENST00000676794.1:c.82+2T>G	ENSP00000504819.1:n.82+2T>G
ENST00000676886.1:c.85-289T>G
ENST00000677191.1:c.403+2T>G
ENST00000677210.1:c.1063+2T>G	ENSP00000503610.1:n.1063+2T>G
ENST00000677220.1:c.132+2467T>G	ENSP00000502987.1:n.132+2467T>G
ENST00000677249.1:c.904+2T>G	ENSP00000503649.1:n.904+2T>G
ENST00000677375.1:c.907+2T>G	ENSP00000503651.1:n.907+2T>G
ENST00000677385.1:c.*1251T>G	ENSP00000502985.1:n.*1251T>G
ENST00000677778.1:c.75+1095T>G
ENST00000677840.1:c.156+2T>G
ENST00000678077.1:c.772+2T>G	ENSP00000504814.1:n.772+2T>G
ENST00000678212.1:c.251+2T>G
ENST00000678365.1:n.49-2693T>G
ENST00000678412.1:c.157-289T>G
ENST00000678418.1:n.1259+2T>G
ENST00000678448.1:c.255+2T>G	ENSP00000503619.1:n.255+2T>G
ENST00000678456.1:c.76-289T>G
ENST00000678970.1:c.232+2T>G
ENST00000679026.1:c.156+2T>G
ENST00000679079.1:c.157-580T>G
ENST00000679228.1:n.1258+2T>G
ENST00000679273.1:c.243+2T>G	ENSP00000504626.1:n.243+2T>G
ENST00000679344.1:c.264+2T>G
ENST00000330752.12:c.868+2T>G	ENSP00000333504.8:n.868+2T>G
ENST00000340913.10:c.1063+2T>G	ENSP00000341826.6:n.1063+2T>G
ENST00000546500.5:c.907+2T>G	ENSP00000448617.1:n.907+2T>G
ENST00000547276.5:c.748+2T>G	ENSP00000447260.1:n.748+2T>G
ENST00000547566.5:c.907+2T>G	ENSP00000449913.1:n.907+2T>G
ENST00000550482.1:c.520+2T>G	ENSP00000446486.1:n.520+2T>G
ENST00000551679.1:n.245+2T>G
NM_002136.2:c.907+2T>G	NP_002127.1:n.907+2T>G
NM_031157.2:c.1063+2T>G	NP_112420.1:n.1063+2T>G
XM_005268826.1:c.1063+2T>G	XP_005268883.1:n.1063+2T>G
XR_245923.1:n.1175+2T>G
XR_245924.1:n.1019+2T>G
NM_002136.3:c.907+2T>G	NP_002127.1:n.907+2T>G
NM_031157.3:c.1063+2T>G	NP_112420.1:n.1063+2T>G
NR_135167.1:n.1025+2T>G
XM_005268826.2:c.1063+2T>G	XP_005268883.1:n.1063+2T>G
XR_245923.2:n.1135+2T>G
NM_002136.4:c.907+2T>G	NP_002127.1:n.907+2T>G
NM_031157.4:c.1063+2T>G MANE Select	NP_112420.1:n.1063+2T>G
NR_135167.2:n.989+2T>G