Canonical Allele Identifier: CA11952345
Gene: DOCK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.169647052C>T , CM000667.2:g.169647052C>T GRCh38
NC_000005.9:g.169074056C>T , CM000667.1:g.169074056C>T GRCh37
NC_000005.8:g.169006634C>T NCBI36
NG_051800.1:g.14806C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000519628.2:c.44-7351C>T ENSP00000428841.2:n.44-7351C>T
ENST00000522138.2:c.44-7351C>T ENSP00000512484.1:n.44-7351C>T
ENST00000520908.7:c.44-7351C>T MANE Select ENSP00000429283.3:n.44-7351C>T
ENST00000648741.1:n.103-7351C>T
ENST00000256935.12:c.44-7351C>T ENSP00000256935.8:n.44-7351C>T
ENST00000522138.1:n.85-7351C>T
ENST00000524185.5:c.44-7351C>T ENSP00000428850.1:n.44-7351C>T
NM_004946.2:c.44-7351C>T NP_004937.1:n.44-7351C>T
XM_005265830.2:c.44-7351C>T XP_005265887.1:n.44-7351C>T
XM_011534448.1:c.44-7351C>T XP_011532750.1:n.44-7351C>T
XM_011534449.1:c.44-7351C>T XP_011532751.1:n.44-7351C>T
XM_011534450.1:c.44-7351C>T XP_011532752.1:n.44-7351C>T
XM_011534451.1:c.44-7351C>T XP_011532753.1:n.44-7351C>T
XR_941089.1:n.124-7351C>T
NM_004946.3:c.44-7351C>T MANE Select NP_004937.1:n.44-7351C>T
NR_156756.1:n.96-7351C>T
XM_005265830.4:c.44-7351C>T XP_005265887.1:n.44-7351C>T
XM_011534448.2:c.44-7351C>T XP_011532750.1:n.44-7351C>T
XM_011534449.2:c.44-7351C>T XP_011532751.1:n.44-7351C>T
XM_011534450.2:c.44-7351C>T XP_011532752.1:n.44-7351C>T
XM_011534451.2:c.44-7351C>T XP_011532753.1:n.44-7351C>T
XM_017009189.1:c.44-7351C>T XP_016864678.1:n.44-7351C>T
XM_017009190.2:c.44-7351C>T XP_016864679.1:n.44-7351C>T