Canonical Allele Identifier: CA372760638

Gene: DOCK8

Linked Data

• MyVariant Identifiers: chr9:g.414865C>T (hg19) ; chr9:g.414865C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.414865C>T , CM000671.2:g.414865C>T	GRCh38
NC_000009.11:g.414865C>T , CM000671.1:g.414865C>T	GRCh37
NC_000009.10:g.404865C>T	NCBI36
NG_017007.1:g.205001C>T , LRG_196:g.205001C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382329.2:c.3314C>T	ENSP00000371766.2:p.Pro1105Leu
ENST00000683406.1:n.135C>T
ENST00000685949.1:n.2402C>T
ENST00000432829.7:c.3614C>T MANE Select	ENSP00000394888.3:p.Pro1205Leu
ENST00000382329.1:c.2015C>T	ENSP00000371766.1:p.Pro672Leu
ENST00000432829.6:c.3614C>T	ENSP00000394888.3:p.Pro1205Leu
ENST00000453981.5:c.3410C>T	ENSP00000408464.2:p.Pro1137Leu
ENST00000469391.5:c.3314C>T	ENSP00000419438.1:p.Pro1105Leu
ENST00000495184.5:n.5569C>T
NM_001190458.1:c.3314C>T	NP_001177387.1:p.Pro1105Leu
NM_001193536.1:c.3410C>T	NP_001180465.1:p.Pro1137Leu
NM_203447.3:c.3614C>T , LRG_196t1:c.3614C>T	NP_982272.2:p.Pro1205Leu
XM_011518045.1:c.3314C>T	XP_011516347.1:p.Pro1105Leu
XM_011518046.1:c.3476C>T	XP_011516348.1:p.Pro1159Leu
XM_011518047.1:c.3410C>T	XP_011516349.1:p.Pro1137Leu
XM_011518048.1:c.3410C>T	XP_011516350.1:p.Pro1137Leu
XM_011518049.1:c.1850C>T	XP_011516351.1:p.Pro617Leu
XM_011518045.3:c.3314C>T	XP_011516347.1:p.Pro1105Leu
XM_011518046.2:c.3476C>T	XP_011516348.1:p.Pro1159Leu
XM_011518047.3:c.3410C>T	XP_011516349.1:p.Pro1137Leu
XM_011518048.2:c.3410C>T	XP_011516350.1:p.Pro1137Leu
XM_011518049.2:c.1850C>T	XP_011516351.1:p.Pro617Leu
XM_017015173.1:c.3410C>T	XP_016870662.1:p.Pro1137Leu
XM_017015174.1:c.3476C>T	XP_016870663.1:p.Pro1159Leu
NM_001190458.2:c.3314C>T	NP_001177387.1:p.Pro1105Leu
NM_001193536.2:c.3410C>T	NP_001180465.1:p.Pro1137Leu
NM_203447.4:c.3614C>T MANE Select	NP_982272.2:p.Pro1205Leu