Canonical Allele Identifier: CA1548136565

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875519_56875527delinsAACTGTTTT , CM000667.2:g.56875519_56875527delinsAACTGTTTT	GRCh38
NC_000005.9:g.56171346_56171354delinsAACTGTTTT , CM000667.1:g.56171346_56171354delinsAACTGTTTT	GRCh37
NC_000005.8:g.56207103_56207111delinsAACTGTTTT	NCBI36
NG_031884.1:g.65447_65455delinsAACTGTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.1965+209_1965+217delinsAACTGTTTT MANE Select	ENSP00000382423.3:n.1965+209_1965+217delinsAACTGTTTT
ENST00000399503.3:c.1965+209_1965+217delinsAACTGTTTT	ENSP00000382423.3:n.1965+209_1965+217delinsAACTGTTTT
NM_005921.1:c.1965+209_1965+217delinsAACTGTTTT	NP_005912.1:n.1965+209_1965+217delinsAACTGTTTT
XM_005248519.3:c.1587+209_1587+217delinsAACTGTTTT	XP_005248576.2:n.1587+209_1587+217delinsAACTGTTTT
XM_011543406.1:c.1710+209_1710+217delinsAACTGTTTT	XP_011541708.1:n.1710+209_1710+217delinsAACTGTTTT
XM_011543407.1:c.1686+2514_1686+2522delinsAACTGTTTT	XP_011541709.1:n.1686+2514_1686+2522delinsAACTGTTTT
XM_011543408.1:c.1965+209_1965+217delinsAACTGTTTT	XP_011541710.1:n.1965+209_1965+217delinsAACTGTTTT
XM_017009484.1:c.1554+209_1554+217delinsAACTGTTTT	XP_016864973.1:n.1554+209_1554+217delinsAACTGTTTT
XM_017009485.1:c.1476+209_1476+217delinsAACTGTTTT	XP_016864974.1:n.1476+209_1476+217delinsAACTGTTTT
XR_001742068.2:n.1996+209_1996+217delinsAACTGTTTT
NM_005921.2:c.1965+209_1965+217delinsAACTGTTTT MANE Select	NP_005912.1:n.1965+209_1965+217delinsAACTGTTTT