Canonical Allele Identifier: CA1548129296

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859973_56859974delinsCA , CM000667.2:g.56859973_56859974delinsCA	GRCh38
NC_000005.9:g.56155800_56155801delinsCA , CM000667.1:g.56155800_56155801delinsCA	GRCh37
NC_000005.8:g.56191557_56191558delinsCA	NCBI36
NG_031884.1:g.49901_49902delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.834+58_834+59delinsCA MANE Select	ENSP00000382423.3:n.834+58_834+59delinsCA
ENST00000399503.3:c.834+58_834+59delinsCA	ENSP00000382423.3:n.834+58_834+59delinsCA
NM_005921.1:c.834+58_834+59delinsCA	NP_005912.1:n.834+58_834+59delinsCA
XM_005248519.3:c.456+58_456+59delinsCA	XP_005248576.2:n.456+58_456+59delinsCA
XM_011543406.1:c.579+58_579+59delinsCA	XP_011541708.1:n.579+58_579+59delinsCA
XM_011543407.1:c.834+58_834+59delinsCA	XP_011541709.1:n.834+58_834+59delinsCA
XM_011543408.1:c.834+58_834+59delinsCA	XP_011541710.1:n.834+58_834+59delinsCA
XM_017009484.1:c.423+58_423+59delinsCA	XP_016864973.1:n.423+58_423+59delinsCA
XM_017009485.1:c.345+58_345+59delinsCA	XP_016864974.1:n.345+58_345+59delinsCA
XR_001742068.2:n.865+58_865+59delinsCA
NM_005921.2:c.834+58_834+59delinsCA MANE Select	NP_005912.1:n.834+58_834+59delinsCA