Canonical Allele Identifier: CA1829649979

Gene: JAK2 INSL6

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.5071030C= , CM000671.2:g.5071030C=	GRCh38
NC_000009.11:g.5071030C= , CM000671.1:g.5071030C=	GRCh37
NC_000009.10:g.5061030C=	NCBI36
NG_009904.1:g.90786C= , LRG_612:g.90786C=
NG_046969.1:g.119681G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000381652.4:c.1641+978C= (JAK2) MANE Select	ENSP00000371067.4:n.1641+978C=
ENST00000636127.1:c.1641+978C= (JAK2)	ENSP00000489812.1:n.1641+978C=
ENST00000381652.3:c.1641+978C= (JAK2)	ENSP00000371067.3:n.1641+978C=
NM_004972.3:c.1641+978C= , LRG_612t1:c.1641+978C= (JAK2)	NP_004963.1:n.1641+978C=
XM_011517701.1:c.377-55686G= (INSL6)	XP_011516003.1:n.377-55686G=
XM_011517702.1:c.377-78597G= (INSL6)	XP_011516004.1:n.377-78597G=
XR_929169.1:n.485-55686G= (INSL6)
NM_001322194.1:c.1641+978C= (JAK2)	NP_001309123.1:n.1641+978C=
NM_001322195.1:c.1641+978C= (JAK2)	NP_001309124.1:n.1641+978C=
NM_001322196.1:c.1641+978C= (JAK2)	NP_001309125.1:n.1641+978C=
NM_001322198.1:c.426+978C= (JAK2)	NP_001309127.1:n.426+978C=
NM_001322199.1:c.426+978C= (JAK2)	NP_001309128.1:n.426+978C=
NM_001322204.1:c.1194+978C= (JAK2)	NP_001309133.1:n.1194+978C=
XM_011517702.3:c.377-78597G= (INSL6)	XP_011516004.1:n.377-78597G=
NM_004972.4:c.1641+978C= (JAK2) MANE Select	NP_004963.1:n.1641+978C=
NM_001322194.2:c.1641+978C= (JAK2)	NP_001309123.1:n.1641+978C=
NM_001322195.2:c.1641+978C= (JAK2)	NP_001309124.1:n.1641+978C=
NM_001322196.2:c.1641+978C= (JAK2)	NP_001309125.1:n.1641+978C=
NM_001322198.2:c.426+978C= (JAK2)	NP_001309127.1:n.426+978C=
NM_001322199.2:c.426+978C= (JAK2)	NP_001309128.1:n.426+978C=
NM_001322204.2:c.1194+978C= (JAK2)	NP_001309133.1:n.1194+978C=
NR_169763.1:n.2125+978C= (JAK2)
NR_169764.1:n.2042+978C= (JAK2)