Canonical Allele Identifier: CA421592987

Gene: ACKR1

Linked Data

• MyVariant Identifiers: chr1:g.159175529A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159205739A>C , CM000663.2:g.159205739A>C	GRCh38
NC_000001.10:g.159175529A>C , CM000663.1:g.159175529A>C	GRCh37
NC_000001.9:g.157442153A>C	NCBI36
NG_011626.1:g.6020A>C
NG_011626.3:g.6727A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000368121.6:c.306A>C	ENSP00000357103.2:p.Ala102=
ENST00000368122.4:c.300A>C MANE Select	ENSP00000357104.1:p.Ala100=
ENST00000435307.2:n.481A>C
ENST00000368121.3:c.306A>C	ENSP00000357103.2:p.Ala102=
ENST00000368122.2:c.300A>C	ENSP00000357104.1:p.Ala100=
ENST00000435307.1:c.306A>C	ENSP00000398406.1:p.Ala102=
ENST00000537147.5:c.300A>C	ENSP00000441985.1:p.Ala100=
NM_001122951.2:c.306A>C	NP_001116423.1:p.Ala102=
NM_002036.3:c.300A>C	NP_002027.2:p.Ala100=
NM_002036.4:c.300A>C MANE Select	NP_002027.2:p.Ala100=
NM_001122951.3:c.306A>C	NP_001116423.1:p.Ala102=