Canonical Allele Identifier: CA1548139161

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881424_56881425delinsTG , CM000667.2:g.56881424_56881425delinsTG	GRCh38
NC_000005.9:g.56177251_56177252delinsTG , CM000667.1:g.56177251_56177252delinsTG	GRCh37
NC_000005.8:g.56213008_56213009delinsTG	NCBI36
NG_031884.1:g.71352_71353delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.2370-146_2370-145delinsTG MANE Select	ENSP00000382423.3:n.2370-146_2370-145delinsTG
ENST00000399503.3:c.2370-146_2370-145delinsTG	ENSP00000382423.3:n.2370-146_2370-145delinsTG
NM_005921.1:c.2370-146_2370-145delinsTG	NP_005912.1:n.2370-146_2370-145delinsTG
XM_005248519.3:c.1992-146_1992-145delinsTG	XP_005248576.2:n.1992-146_1992-145delinsTG
XM_011543406.1:c.2115-146_2115-145delinsTG	XP_011541708.1:n.2115-146_2115-145delinsTG
XM_011543407.1:c.2091-146_2091-145delinsTG	XP_011541709.1:n.2091-146_2091-145delinsTG
XM_011543408.1:c.2370-146_2370-145delinsTG	XP_011541710.1:n.2370-146_2370-145delinsTG
XM_017009484.1:c.1959-146_1959-145delinsTG	XP_016864973.1:n.1959-146_1959-145delinsTG
XM_017009485.1:c.1881-146_1881-145delinsTG	XP_016864974.1:n.1881-146_1881-145delinsTG
XR_001742068.2:n.2401-146_2401-145delinsTG
NM_005921.2:c.2370-146_2370-145delinsTG MANE Select	NP_005912.1:n.2370-146_2370-145delinsTG