Canonical Allele Identifier: CA1548129155

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859667_56859668delinsAC , CM000667.2:g.56859667_56859668delinsAC	GRCh38
NC_000005.9:g.56155494_56155495delinsAC , CM000667.1:g.56155494_56155495delinsAC	GRCh37
NC_000005.8:g.56191251_56191252delinsAC	NCBI36
NG_031884.1:g.49595_49596delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.634-48_634-47delinsAC MANE Select	ENSP00000382423.3:n.634-48_634-47delinsAC
ENST00000399503.3:c.634-48_634-47delinsAC	ENSP00000382423.3:n.634-48_634-47delinsAC
NM_005921.1:c.634-48_634-47delinsAC	NP_005912.1:n.634-48_634-47delinsAC
XM_005248519.3:c.256-48_256-47delinsAC	XP_005248576.2:n.256-48_256-47delinsAC
XM_011543406.1:c.379-48_379-47delinsAC	XP_011541708.1:n.379-48_379-47delinsAC
XM_011543407.1:c.634-48_634-47delinsAC	XP_011541709.1:n.634-48_634-47delinsAC
XM_011543408.1:c.634-48_634-47delinsAC	XP_011541710.1:n.634-48_634-47delinsAC
XM_017009484.1:c.223-48_223-47delinsAC	XP_016864973.1:n.223-48_223-47delinsAC
XM_017009485.1:c.145-48_145-47delinsAC	XP_016864974.1:n.145-48_145-47delinsAC
XR_001742068.2:n.665-48_665-47delinsAC
NM_005921.2:c.634-48_634-47delinsAC MANE Select	NP_005912.1:n.634-48_634-47delinsAC