Canonical Allele Identifier: CA812365446

Gene: MAP3K1

Linked Data

• dbSNP Id: rs1339056835
• gnomAD v4: 5-56860000-T-TCA
• MyVariant Identifiers: chr5:g.56155827_56155828insCA (hg19) ; chr5:g.56860000_56860001insCA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56860000_56860001insCA , CM000667.2:g.56860000_56860001insCA	GRCh38
NC_000005.9:g.56155827_56155828insCA , CM000667.1:g.56155827_56155828insCA	GRCh37
NC_000005.8:g.56191584_56191585insCA	NCBI36
NG_031884.1:g.49928_49929insCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.834+85_834+86insCA MANE Select	ENSP00000382423.3:n.834+85_834+86insCA
ENST00000399503.3:c.834+85_834+86insCA	ENSP00000382423.3:n.834+85_834+86insCA
NM_005921.1:c.834+85_834+86insCA	NP_005912.1:n.834+85_834+86insCA
XM_005248519.3:c.456+85_456+86insCA	XP_005248576.2:n.456+85_456+86insCA
XM_011543406.1:c.579+85_579+86insCA	XP_011541708.1:n.579+85_579+86insCA
XM_011543407.1:c.834+85_834+86insCA	XP_011541709.1:n.834+85_834+86insCA
XM_011543408.1:c.834+85_834+86insCA	XP_011541710.1:n.834+85_834+86insCA
XM_017009484.1:c.423+85_423+86insCA	XP_016864973.1:n.423+85_423+86insCA
XM_017009485.1:c.345+85_345+86insCA	XP_016864974.1:n.345+85_345+86insCA
XR_001742068.2:n.865+85_865+86insCA
NM_005921.2:c.834+85_834+86insCA MANE Select	NP_005912.1:n.834+85_834+86insCA