Canonical Allele Identifier: CA1829665149

Gene: JAK2 INSL6

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.5081785T= , CM000671.2:g.5081785T=	GRCh38
NC_000009.11:g.5081785T= , CM000671.1:g.5081785T=	GRCh37
NC_000009.10:g.5071785T=	NCBI36
NG_009904.1:g.101541T= , LRG_612:g.101541T=
NG_046969.1:g.108926A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000381652.4:c.2495T= (JAK2) MANE Select	ENSP00000371067.4:p.Phe832=
ENST00000381652.3:c.2495T= (JAK2)	ENSP00000371067.3:p.Phe832=
NM_004972.3:c.2495T= , LRG_612t1:c.2495T= (JAK2)	NP_004963.1:p.Phe832=
XM_011517701.1:c.377-66441A= (INSL6)	XP_011516003.1:n.377-66441A=
XM_011517702.1:c.376+82394A= (INSL6)	XP_011516004.1:n.376+82394A=
XR_929169.1:n.485-66441A= (INSL6)
NM_001322194.1:c.2495T= (JAK2)	NP_001309123.1:p.Phe832=
NM_001322195.1:c.2495T= (JAK2)	NP_001309124.1:p.Phe832=
NM_001322196.1:c.2495T= (JAK2)	NP_001309125.1:p.Phe832=
NM_001322198.1:c.1280T= (JAK2)	NP_001309127.1:p.Phe427=
NM_001322199.1:c.1280T= (JAK2)	NP_001309128.1:p.Phe427=
NM_001322204.1:c.2048T= (JAK2)	NP_001309133.1:p.Phe683=
XM_011517702.3:c.376+82394A= (INSL6)	XP_011516004.1:n.376+82394A=
NM_004972.4:c.2495T= (JAK2) MANE Select	NP_004963.1:p.Phe832=
NM_001322194.2:c.2495T= (JAK2)	NP_001309123.1:p.Phe832=
NM_001322195.2:c.2495T= (JAK2)	NP_001309124.1:p.Phe832=
NM_001322196.2:c.2495T= (JAK2)	NP_001309125.1:p.Phe832=
NM_001322198.2:c.1280T= (JAK2)	NP_001309127.1:p.Phe427=
NM_001322199.2:c.1280T= (JAK2)	NP_001309128.1:p.Phe427=
NM_001322204.2:c.2048T= (JAK2)	NP_001309133.1:p.Phe683=
NR_169763.1:n.2979T= (JAK2)
NR_169764.1:n.2896T= (JAK2)