Canonical Allele Identifier: CA1548136533

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875461_56875466delinsCTTTTG , CM000667.2:g.56875461_56875466delinsCTTTTG	GRCh38
NC_000005.9:g.56171288_56171293delinsCTTTTG , CM000667.1:g.56171288_56171293delinsCTTTTG	GRCh37
NC_000005.8:g.56207045_56207050delinsCTTTTG	NCBI36
NG_031884.1:g.65389_65394delinsCTTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.1965+151_1965+156delinsCTTTTG MANE Select	ENSP00000382423.3:n.1965+151_1965+156delinsCTTTTG
ENST00000399503.3:c.1965+151_1965+156delinsCTTTTG	ENSP00000382423.3:n.1965+151_1965+156delinsCTTTTG
NM_005921.1:c.1965+151_1965+156delinsCTTTTG	NP_005912.1:n.1965+151_1965+156delinsCTTTTG
XM_005248519.3:c.1587+151_1587+156delinsCTTTTG	XP_005248576.2:n.1587+151_1587+156delinsCTTTTG
XM_011543406.1:c.1710+151_1710+156delinsCTTTTG	XP_011541708.1:n.1710+151_1710+156delinsCTTTTG
XM_011543407.1:c.1686+2456_1686+2461delinsCTTTTG	XP_011541709.1:n.1686+2456_1686+2461delinsCTTTTG
XM_011543408.1:c.1965+151_1965+156delinsCTTTTG	XP_011541710.1:n.1965+151_1965+156delinsCTTTTG
XM_017009484.1:c.1554+151_1554+156delinsCTTTTG	XP_016864973.1:n.1554+151_1554+156delinsCTTTTG
XM_017009485.1:c.1476+151_1476+156delinsCTTTTG	XP_016864974.1:n.1476+151_1476+156delinsCTTTTG
XR_001742068.2:n.1996+151_1996+156delinsCTTTTG
NM_005921.2:c.1965+151_1965+156delinsCTTTTG MANE Select	NP_005912.1:n.1965+151_1965+156delinsCTTTTG