Canonical Allele Identifier: CA2673909448

Gene: MAP3K1

Linked Data

• gnomAD v4: 5-56875390-A-AAT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875392_56875393dup , CM000667.2:g.56875392_56875393dup	GRCh38
NC_000005.9:g.56171219_56171220dup , CM000667.1:g.56171219_56171220dup	GRCh37
NC_000005.8:g.56206976_56206977dup	NCBI36
NG_031884.1:g.65320_65321dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.1965+82_1965+83dup MANE Select	ENSP00000382423.3:n.1965+82_1965+83dup
ENST00000399503.3:c.1965+82_1965+83dup	ENSP00000382423.3:n.1965+82_1965+83dup
NM_005921.1:c.1965+82_1965+83dup	NP_005912.1:n.1965+82_1965+83dup
XM_005248519.3:c.1587+82_1587+83dup	XP_005248576.2:n.1587+82_1587+83dup
XM_011543406.1:c.1710+82_1710+83dup	XP_011541708.1:n.1710+82_1710+83dup
XM_011543407.1:c.1686+2387_1686+2388dup	XP_011541709.1:n.1686+2387_1686+2388dup
XM_011543408.1:c.1965+82_1965+83dup	XP_011541710.1:n.1965+82_1965+83dup
XM_017009484.1:c.1554+82_1554+83dup	XP_016864973.1:n.1554+82_1554+83dup
XM_017009485.1:c.1476+82_1476+83dup	XP_016864974.1:n.1476+82_1476+83dup
XR_001742068.2:n.1996+82_1996+83dup
NM_005921.2:c.1965+82_1965+83dup MANE Select	NP_005912.1:n.1965+82_1965+83dup