Canonical Allele Identifier: CA3273118

Gene: MAP3K1

Linked Data

• dbSNP Id: rs761930383
• ExAC: 5:56178123 C / T
• gnomAD v2: 5-56178123-C-T
• gnomAD v4: 5-56882296-C-T
• MyVariant Identifiers: chr5:g.56178123C>T (hg19) ; chr5:g.56882296C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882296C>T , CM000667.2:g.56882296C>T	GRCh38
NC_000005.9:g.56178123C>T , CM000667.1:g.56178123C>T	GRCh37
NC_000005.8:g.56213880C>T	NCBI36
NG_031884.1:g.72224C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.3096C>T MANE Select	ENSP00000382423.3:p.Asn1032=
ENST00000399503.3:c.3096C>T	ENSP00000382423.3:p.Asn1032=
NM_005921.1:c.3096C>T	NP_005912.1:p.Asn1032=
XM_005248519.3:c.2718C>T	XP_005248576.2:p.Asn906=
XM_011543406.1:c.2841C>T	XP_011541708.1:p.Asn947=
XM_011543407.1:c.2817C>T	XP_011541709.1:p.Asn939=
XM_011543408.1:c.3096C>T	XP_011541710.1:p.Asn1032=
XM_017009484.1:c.2685C>T	XP_016864973.1:p.Asn895=
XM_017009485.1:c.2607C>T	XP_016864974.1:p.Asn869=
XR_001742068.2:n.3127C>T
NM_005921.2:c.3096C>T MANE Select	NP_005912.1:p.Asn1032=