Canonical Allele Identifier: CA1548136534

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875467_56875471delinsTTTTG , CM000667.2:g.56875467_56875471delinsTTTTG	GRCh38
NC_000005.9:g.56171294_56171298delinsTTTTG , CM000667.1:g.56171294_56171298delinsTTTTG	GRCh37
NC_000005.8:g.56207051_56207055delinsTTTTG	NCBI36
NG_031884.1:g.65395_65399delinsTTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.1965+157_1965+161delinsTTTTG MANE Select	ENSP00000382423.3:n.1965+157_1965+161delinsTTTTG
ENST00000399503.3:c.1965+157_1965+161delinsTTTTG	ENSP00000382423.3:n.1965+157_1965+161delinsTTTTG
NM_005921.1:c.1965+157_1965+161delinsTTTTG	NP_005912.1:n.1965+157_1965+161delinsTTTTG
XM_005248519.3:c.1587+157_1587+161delinsTTTTG	XP_005248576.2:n.1587+157_1587+161delinsTTTTG
XM_011543406.1:c.1710+157_1710+161delinsTTTTG	XP_011541708.1:n.1710+157_1710+161delinsTTTTG
XM_011543407.1:c.1686+2462_1686+2466delinsTTTTG	XP_011541709.1:n.1686+2462_1686+2466delinsTTTTG
XM_011543408.1:c.1965+157_1965+161delinsTTTTG	XP_011541710.1:n.1965+157_1965+161delinsTTTTG
XM_017009484.1:c.1554+157_1554+161delinsTTTTG	XP_016864973.1:n.1554+157_1554+161delinsTTTTG
XM_017009485.1:c.1476+157_1476+161delinsTTTTG	XP_016864974.1:n.1476+157_1476+161delinsTTTTG
XR_001742068.2:n.1996+157_1996+161delinsTTTTG
NM_005921.2:c.1965+157_1965+161delinsTTTTG MANE Select	NP_005912.1:n.1965+157_1965+161delinsTTTTG