Canonical Allele Identifier: CA2673908351

Gene: MAP3K1

Linked Data

• gnomAD v4: 5-56859664-CTTACCTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859668_56859674del , CM000667.2:g.56859668_56859674del	GRCh38
NC_000005.9:g.56155495_56155501del , CM000667.1:g.56155495_56155501del	GRCh37
NC_000005.8:g.56191252_56191258del	NCBI36
NG_031884.1:g.49596_49602del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.634-47_634-41del MANE Select	ENSP00000382423.3:n.634-47_634-41del
ENST00000399503.3:c.634-47_634-41del	ENSP00000382423.3:n.634-47_634-41del
NM_005921.1:c.634-47_634-41del	NP_005912.1:n.634-47_634-41del
XM_005248519.3:c.256-47_256-41del	XP_005248576.2:n.256-47_256-41del
XM_011543406.1:c.379-47_379-41del	XP_011541708.1:n.379-47_379-41del
XM_011543407.1:c.634-47_634-41del	XP_011541709.1:n.634-47_634-41del
XM_011543408.1:c.634-47_634-41del	XP_011541710.1:n.634-47_634-41del
XM_017009484.1:c.223-47_223-41del	XP_016864973.1:n.223-47_223-41del
XM_017009485.1:c.145-47_145-41del	XP_016864974.1:n.145-47_145-41del
XR_001742068.2:n.665-47_665-41del
NM_005921.2:c.634-47_634-41del MANE Select	NP_005912.1:n.634-47_634-41del