Allele Registry

Canonical Allele Identifier: CA10782358

Gene: CD244 HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr1:g.160839213G>A

GRCh37 chr1:g.160809003G>A

Linked Data - Sequence & Population

gnomAD v2:

1:160809003 G / A

gnomAD v3:

1:160839213 G / A

gnomAD v4:

chr1-160839213-G-A

Joint Max Group AF 0.56374189 (AMR)

Genomes Max Group AF 0.55534515 (NFE)

Exomes Max Group AF 0.58376235 (AMR)

Linked Data - NCBI & NCI

dbSNP:

6682654

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160839213G>A , CM000663.2:g.160839213G>A	GRCh38
NC_000001.10:g.160809003G>A , CM000663.1:g.160809003G>A	GRCh37
NC_000001.9:g.159075627G>A	NCBI36
NG_015991.1:g.28690C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368034.9:c.656-164C>T MANE Select	ENSP00000357013.4:n.656-164C>T
ENST00000322302.7:c.380-164C>T	ENSP00000313619.7:n.380-164C>T
ENST00000368033.7:c.671-164C>T	ENSP00000357012.3:n.671-164C>T
ENST00000368034.8:c.656-164C>T	ENSP00000357013.4:n.656-164C>T
ENST00000492063.5:c.656-164C>T	ENSP00000432636.1:n.656-164C>T
NM_001166663.1:c.671-164C>T	NP_001160135.1:n.671-164C>T
NM_001166664.1:c.380-164C>T	NP_001160136.1:n.380-164C>T
NM_016382.3:c.656-164C>T	NP_057466.1:n.656-164C>T
XM_011509620.1:c.671-164C>T	XP_011507922.1:n.671-164C>T
XM_011509621.1:c.671-164C>T	XP_011507923.1:n.671-164C>T
XM_011509622.1:c.656-164C>T	XP_011507924.1:n.656-164C>T
XM_011509623.1:c.62-164C>T	XP_011507925.1:n.62-164C>T
XM_011509621.2:c.671-164C>T	XP_011507923.1:n.671-164C>T
XM_011509622.2:c.656-164C>T	XP_011507924.1:n.656-164C>T
XM_011509623.3:c.62-164C>T	XP_011507925.1:n.62-164C>T
XR_001737229.1:n.881-164C>T
NM_016382.4:c.656-164C>T MANE Select	NP_057466.1:n.656-164C>T
NM_001166663.2:c.671-164C>T	NP_001160135.1:n.671-164C>T
NM_001166664.2:c.380-164C>T	NP_001160136.1:n.380-164C>T

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