Canonical Allele Identifier: CA463691058

Gene: DOCK8

Linked Data

• MyVariant Identifiers: chr9:g.414851A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.414851A>T , CM000671.2:g.414851A>T	GRCh38
NC_000009.11:g.414851A>T , CM000671.1:g.414851A>T	GRCh37
NC_000009.10:g.404851A>T	NCBI36
NG_017007.1:g.204987A>T , LRG_196:g.204987A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382329.2:c.3300A>T	ENSP00000371766.2:p.Pro1100=
ENST00000683406.1:n.121A>T
ENST00000685949.1:n.2388A>T
ENST00000432829.7:c.3600A>T MANE Select	ENSP00000394888.3:p.Pro1200=
ENST00000382329.1:c.2001A>T	ENSP00000371766.1:p.Pro667=
ENST00000432829.6:c.3600A>T	ENSP00000394888.3:p.Pro1200=
ENST00000453981.5:c.3396A>T	ENSP00000408464.2:p.Pro1132=
ENST00000469391.5:c.3300A>T	ENSP00000419438.1:p.Pro1100=
ENST00000495184.5:n.5555A>T
NM_001190458.1:c.3300A>T	NP_001177387.1:p.Pro1100=
NM_001193536.1:c.3396A>T	NP_001180465.1:p.Pro1132=
NM_203447.3:c.3600A>T , LRG_196t1:c.3600A>T	NP_982272.2:p.Pro1200=
XM_011518045.1:c.3300A>T	XP_011516347.1:p.Pro1100=
XM_011518046.1:c.3462A>T	XP_011516348.1:p.Pro1154=
XM_011518047.1:c.3396A>T	XP_011516349.1:p.Pro1132=
XM_011518048.1:c.3396A>T	XP_011516350.1:p.Pro1132=
XM_011518049.1:c.1836A>T	XP_011516351.1:p.Pro612=
XM_011518045.3:c.3300A>T	XP_011516347.1:p.Pro1100=
XM_011518046.2:c.3462A>T	XP_011516348.1:p.Pro1154=
XM_011518047.3:c.3396A>T	XP_011516349.1:p.Pro1132=
XM_011518048.2:c.3396A>T	XP_011516350.1:p.Pro1132=
XM_011518049.2:c.1836A>T	XP_011516351.1:p.Pro612=
XM_017015173.1:c.3396A>T	XP_016870662.1:p.Pro1132=
XM_017015174.1:c.3462A>T	XP_016870663.1:p.Pro1154=
NM_001190458.2:c.3300A>T	NP_001177387.1:p.Pro1100=
NM_001193536.2:c.3396A>T	NP_001180465.1:p.Pro1132=
NM_203447.4:c.3600A>T MANE Select	NP_982272.2:p.Pro1200=