Canonical Allele Identifier: CA10902832

Gene: AK4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.65167814T>C , CM000663.2:g.65167814T>C	GRCh38
NC_000001.10:g.65633497T>C , CM000663.1:g.65633497T>C	GRCh37
NC_000001.9:g.65406085T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327299.8:c.145+19262T>C MANE Select	ENSP00000322175.7:n.145+19262T>C
ENST00000327299.7:c.145+19262T>C	ENSP00000322175.7:n.145+19262T>C
ENST00000395334.6:c.145+19262T>C	ENSP00000378743.2:n.145+19262T>C
ENST00000470888.6:n.664+19262T>C
ENST00000474968.5:n.139+18674T>C
ENST00000479060.1:n.88+1795T>C
ENST00000497030.5:n.392+19262T>C
ENST00000545314.5:c.145+19262T>C	ENSP00000445912.1:n.145+19262T>C
ENST00000546702.5:c.-12+20051T>C	ENSP00000448458.1:n.-12+20051T>C
NM_001005353.2:c.145+19262T>C	NP_001005353.1:n.145+19262T>C
NM_013410.3:c.145+19262T>C	NP_037542.1:n.145+19262T>C
NM_203464.2:c.145+19262T>C	NP_982289.1:n.145+19262T>C
NM_001330616.1:c.-12+18674T>C	NP_001317545.1:n.-12+18674T>C
XM_017000613.1:c.-12+20149T>C	XP_016856102.1:n.-12+20149T>C
NM_013410.4:c.145+19262T>C MANE Select	NP_037542.1:n.145+19262T>C
NM_001330616.2:c.-12+18674T>C	NP_001317545.1:n.-12+18674T>C
NM_001005353.3:c.145+19262T>C	NP_001005353.1:n.145+19262T>C
NM_203464.3:c.145+19262T>C	NP_982289.1:n.145+19262T>C