Canonical Allele Identifier: CA31606935
Gene: CD244 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160860478A>G , CM000663.2:g.160860478A>G GRCh38
NC_000001.10:g.160830268A>G , CM000663.1:g.160830268A>G GRCh37
NC_000001.9:g.159096892A>G NCBI36
NG_015991.1:g.7425T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368034.9:c.61+2139T>C MANE Select ENSP00000357013.4:n.61+2139T>C
ENST00000322302.7:c.61+2139T>C ENSP00000313619.7:n.61+2139T>C
ENST00000368033.7:c.61+2139T>C ENSP00000357012.3:n.61+2139T>C
ENST00000368034.8:c.61+2139T>C ENSP00000357013.4:n.61+2139T>C
ENST00000492063.5:c.61+2139T>C ENSP00000432636.1:n.61+2139T>C
NM_001166663.1:c.61+2139T>C NP_001160135.1:n.61+2139T>C
NM_001166664.1:c.61+2139T>C NP_001160136.1:n.61+2139T>C
NM_016382.3:c.61+2139T>C NP_057466.1:n.61+2139T>C
XM_011509620.1:c.61+2139T>C XP_011507922.1:n.61+2139T>C
XM_011509621.1:c.61+2139T>C XP_011507923.1:n.61+2139T>C
XM_011509622.1:c.61+2139T>C XP_011507924.1:n.61+2139T>C
XM_011509623.1:c.61+2139T>C XP_011507925.1:n.61+2139T>C
XM_011509621.2:c.61+2139T>C XP_011507923.1:n.61+2139T>C
XM_011509622.2:c.61+2139T>C XP_011507924.1:n.61+2139T>C
XM_011509623.3:c.61+2139T>C XP_011507925.1:n.61+2139T>C
XR_001737229.1:n.271+2139T>C
NM_016382.4:c.61+2139T>C MANE Select NP_057466.1:n.61+2139T>C
NM_001166663.2:c.61+2139T>C NP_001160135.1:n.61+2139T>C
NM_001166664.2:c.61+2139T>C NP_001160136.1:n.61+2139T>C
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