Canonical Allele Identifier: CA343057707

Gene: ACKR1

Linked Data

• dbSNP Id: rs34599082
• gnomAD v3: 1-159205704-C-A
• gnomAD v4: 1-159205704-C-A
• COSMIC: COSM4938018 ; COSM4938019
• MyVariant Identifiers: chr1:g.159175494C>A (hg19) ; chr1:g.159205704C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159205704C>A , CM000663.2:g.159205704C>A	GRCh38
NC_000001.10:g.159175494C>A , CM000663.1:g.159175494C>A	GRCh37
NC_000001.9:g.157442118C>A	NCBI36
NG_011626.1:g.5985C>A
NG_011626.3:g.6692C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000368121.6:c.271C>A	ENSP00000357103.2:p.Arg91Ser
ENST00000368122.4:c.265C>A MANE Select	ENSP00000357104.1:p.Arg89Ser
ENST00000435307.2:n.446C>A
ENST00000368121.3:c.271C>A	ENSP00000357103.2:p.Arg91Ser
ENST00000368122.2:c.265C>A	ENSP00000357104.1:p.Arg89Ser
ENST00000435307.1:c.271C>A	ENSP00000398406.1:p.Arg91Ser
ENST00000537147.5:c.265C>A	ENSP00000441985.1:p.Arg89Ser
NM_001122951.2:c.271C>A	NP_001116423.1:p.Arg91Ser
NM_002036.3:c.265C>A	NP_002027.2:p.Arg89Ser
NM_002036.4:c.265C>A MANE Select	NP_002027.2:p.Arg89Ser
NM_001122951.3:c.271C>A	NP_001116423.1:p.Arg91Ser