Canonical Allele Identifier: CA3272611

Gene: MAP3K1

Linked Data

• dbSNP Id: rs767923471
• ExAC: 5:56155740 C / T
• gnomAD v2: 5-56155740-C-T
• gnomAD v3: 5-56859913-C-T
• gnomAD v4: 5-56859913-C-T
• MyVariant Identifiers: chr5:g.56155740C>T (hg19) ; chr5:g.56859913C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859913C>T , CM000667.2:g.56859913C>T	GRCh38
NC_000005.9:g.56155740C>T , CM000667.1:g.56155740C>T	GRCh37
NC_000005.8:g.56191497C>T	NCBI36
NG_031884.1:g.49841C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.832C>T MANE Select	ENSP00000382423.3:p.Pro278Ser
ENST00000399503.3:c.832C>T	ENSP00000382423.3:p.Pro278Ser
NM_005921.1:c.832C>T	NP_005912.1:p.Pro278Ser
XM_005248519.3:c.454C>T	XP_005248576.2:p.Pro152Ser
XM_011543406.1:c.577C>T	XP_011541708.1:p.Pro193Ser
XM_011543407.1:c.832C>T	XP_011541709.1:p.Pro278Ser
XM_011543408.1:c.832C>T	XP_011541710.1:p.Pro278Ser
XM_017009484.1:c.421C>T	XP_016864973.1:p.Pro141Ser
XM_017009485.1:c.343C>T	XP_016864974.1:p.Pro115Ser
XR_001742068.2:n.863C>T
NM_005921.2:c.832C>T MANE Select	NP_005912.1:p.Pro278Ser