Canonical Allele Identifier: CA359787060

Gene: MAP3K1

Linked Data

• gnomAD v3: 5-56882103-A-C
• gnomAD v4: 5-56882103-A-C
• MyVariant Identifiers: chr5:g.56177930A>C (hg19) ; chr5:g.56882103A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882103A>C , CM000667.2:g.56882103A>C	GRCh38
NC_000005.9:g.56177930A>C , CM000667.1:g.56177930A>C	GRCh37
NC_000005.8:g.56213687A>C	NCBI36
NG_031884.1:g.72031A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2903A>C MANE Select	ENSP00000382423.3:p.Asn968Thr
ENST00000399503.3:c.2903A>C	ENSP00000382423.3:p.Asn968Thr
NM_005921.1:c.2903A>C	NP_005912.1:p.Asn968Thr
XM_005248519.3:c.2525A>C	XP_005248576.2:p.Asn842Thr
XM_011543406.1:c.2648A>C	XP_011541708.1:p.Asn883Thr
XM_011543407.1:c.2624A>C	XP_011541709.1:p.Asn875Thr
XM_011543408.1:c.2903A>C	XP_011541710.1:p.Asn968Thr
XM_017009484.1:c.2492A>C	XP_016864973.1:p.Asn831Thr
XM_017009485.1:c.2414A>C	XP_016864974.1:p.Asn805Thr
XR_001742068.2:n.2934A>C
NM_005921.2:c.2903A>C MANE Select	NP_005912.1:p.Asn968Thr