Canonical Allele Identifier: CA1172217764

Gene: AK4

Linked Data

• dbSNP Id: rs1336472

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.65230247G>T , CM000663.2:g.65230247G>T	GRCh38
NC_000001.10:g.65695930G>T , CM000663.1:g.65695930G>T	GRCh37
NC_000001.9:g.65468518G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000327299.8:c.*4070G>T MANE Select	ENSP00000322175.7:n.*4070G>T
ENST00000327299.7:c.*4070G>T	ENSP00000322175.7:n.*4070G>T
ENST00000395334.6:c.*4070G>T	ENSP00000378743.2:n.*4070G>T
ENST00000545314.5:c.*4070G>T	ENSP00000445912.1:n.*4070G>T
NM_001005353.2:c.*4070G>T	NP_001005353.1:n.*4070G>T
NM_013410.3:c.*4070G>T	NP_037542.1:n.*4070G>T
NM_203464.2:c.*4070G>T	NP_982289.1:n.*4070G>T
NM_001330616.1:c.*4070G>T	NP_001317545.1:n.*4070G>T
XM_017000613.1:c.*4070G>T	XP_016856102.1:n.*4070G>T
NM_013410.4:c.*4070G>T MANE Select	NP_037542.1:n.*4070G>T
NM_001330616.2:c.*4070G>T	NP_001317545.1:n.*4070G>T
NM_001005353.3:c.*4070G>T	NP_001005353.1:n.*4070G>T
NM_203464.3:c.*4070G>T	NP_982289.1:n.*4070G>T