Canonical Allele Identifier: CA2665159124
Gene: CX3CR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.39266031_39266048dup , CM000665.2:g.39266031_39266048dup GRCh38
NC_000003.11:g.39307522_39307539dup , CM000665.1:g.39307522_39307539dup GRCh37
NC_000003.10:g.39282526_39282543dup NCBI36
NG_016362.1:g.20695_20712dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000399220.3:c.469_486dup MANE Select ENSP00000382166.3:p.Ala162_Pro163insAlaIleLeuValAlaAla
ENST00000358309.3:c.565_582dup ENSP00000351059.3:p.Ala194_Pro195insAlaIleLeuValAlaAla
ENST00000399220.2:c.469_486dup ENSP00000382166.2:p.Ala162_Pro163insAlaIleLeuValAlaAla
ENST00000435290.1:c.469_486dup ENSP00000394960.1:p.Ala162_Pro163insAlaIleLeuValAlaAla
ENST00000541347.5:c.469_486dup ENSP00000439140.1:p.Ala162_Pro163insAlaIleLeuValAlaAla
ENST00000542107.5:c.469_486dup ENSP00000444928.1:p.Ala162_Pro163insAlaIleLeuValAlaAla
NM_001171171.1:c.469_486dup NP_001164642.1:p.Ala162_Pro163insAlaIleLeuValAlaAla
NM_001171172.1:c.469_486dup NP_001164643.1:p.Ala162_Pro163insAlaIleLeuValAlaAla
NM_001171174.1:c.565_582dup NP_001164645.1:p.Ala194_Pro195insAlaIleLeuValAlaAla
NM_001337.3:c.469_486dup NP_001328.1:p.Ala162_Pro163insAlaIleLeuValAlaAla
NM_001337.4:c.469_486dup MANE Select NP_001328.1:p.Ala162_Pro163insAlaIleLeuValAlaAla
NM_001171171.2:c.469_486dup NP_001164642.1:p.Ala162_Pro163insAlaIleLeuValAlaAla
NM_001171172.2:c.469_486dup NP_001164643.1:p.Ala162_Pro163insAlaIleLeuValAlaAla