Canonical Allele Identifier: CA3273128

Gene: MAP3K1

Linked Data

• dbSNP Id: rs756800659
• ExAC: 5:56178210 G / C
• gnomAD v2: 5-56178210-G-C
• gnomAD v4: 5-56882383-G-C
• MyVariant Identifiers: chr5:g.56178210G>C (hg19) ; chr5:g.56882383G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882383G>C , CM000667.2:g.56882383G>C	GRCh38
NC_000005.9:g.56178210G>C , CM000667.1:g.56178210G>C	GRCh37
NC_000005.8:g.56213967G>C	NCBI36
NG_031884.1:g.72311G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3183G>C MANE Select	ENSP00000382423.3:p.Lys1061Asn
ENST00000399503.3:c.3183G>C	ENSP00000382423.3:p.Lys1061Asn
NM_005921.1:c.3183G>C	NP_005912.1:p.Lys1061Asn
XM_005248519.3:c.2805G>C	XP_005248576.2:p.Lys935Asn
XM_011543406.1:c.2928G>C	XP_011541708.1:p.Lys976Asn
XM_011543407.1:c.2904G>C	XP_011541709.1:p.Lys968Asn
XM_011543408.1:c.3183G>C	XP_011541710.1:p.Lys1061Asn
XM_017009484.1:c.2772G>C	XP_016864973.1:p.Lys924Asn
XM_017009485.1:c.2694G>C	XP_016864974.1:p.Lys898Asn
XR_001742068.2:n.3214G>C
NM_005921.2:c.3183G>C MANE Select	NP_005912.1:p.Lys1061Asn