Canonical Allele Identifier: CA4972043

Linked Data

dbSNP Id: rs776347825

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.5078368_5078370del , CM000671.2:g.5078368_5078370del GRCh38
NC_000009.11:g.5078368_5078370del , CM000671.1:g.5078368_5078370del GRCh37
NC_000009.10:g.5068368_5068370del NCBI36
NG_009904.1:g.98124_98126del , LRG_612:g.98124_98126del
NG_046969.1:g.112347_112349del

Transcript Alleles

HGVS Amino-acid change
ENST00000381652.4:c.2055_2057del (JAK2) MANE Select ENSP00000371067.4:p.Glu685del
ENST00000636127.1:c.2055_2057del (JAK2) ENSP00000489812.1:p.Glu685del
ENST00000381652.3:c.2055_2057del (JAK2) ENSP00000371067.3:p.Glu685del
NM_004972.3:c.2055_2057del , LRG_612t1:c.2055_2057del (JAK2) NP_004963.1:p.Glu685del
XM_011517701.1:c.377-63020_377-63018del (INSL6) XP_011516003.1:n.377-63020_377-63018del
XM_011517702.1:c.376+85815_376+85817del (INSL6) XP_011516004.1:n.376+85815_376+85817del
XR_929169.1:n.485-63020_485-63018del (INSL6)
NM_001322194.1:c.2055_2057del (JAK2) NP_001309123.1:p.Glu685del
NM_001322195.1:c.2055_2057del (JAK2) NP_001309124.1:p.Glu685del
NM_001322196.1:c.2055_2057del (JAK2) NP_001309125.1:p.Glu685del
NM_001322198.1:c.840_842del (JAK2) NP_001309127.1:p.Glu280del
NM_001322199.1:c.840_842del (JAK2) NP_001309128.1:p.Glu280del
NM_001322204.1:c.1608_1610del (JAK2) NP_001309133.1:p.Glu536del
XM_011517702.3:c.376+85815_376+85817del (INSL6) XP_011516004.1:n.376+85815_376+85817del
NM_004972.4:c.2055_2057del (JAK2) MANE Select NP_004963.1:p.Glu685del
NM_001322194.2:c.2055_2057del (JAK2) NP_001309123.1:p.Glu685del
NM_001322195.2:c.2055_2057del (JAK2) NP_001309124.1:p.Glu685del
NM_001322196.2:c.2055_2057del (JAK2) NP_001309125.1:p.Glu685del
NM_001322198.2:c.840_842del (JAK2) NP_001309127.1:p.Glu280del
NM_001322199.2:c.840_842del (JAK2) NP_001309128.1:p.Glu280del
NM_001322204.2:c.1608_1610del (JAK2) NP_001309133.1:p.Glu536del
NR_169763.1:n.2539_2541del (JAK2)
NR_169764.1:n.2456_2458del (JAK2)