Canonical Allele Identifier: CA359802632

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56155699C>T (hg19) ; chr5:g.56859872C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859872C>T , CM000667.2:g.56859872C>T	GRCh38
NC_000005.9:g.56155699C>T , CM000667.1:g.56155699C>T	GRCh37
NC_000005.8:g.56191456C>T	NCBI36
NG_031884.1:g.49800C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.791C>T MANE Select	ENSP00000382423.3:p.Ser264Leu
ENST00000399503.3:c.791C>T	ENSP00000382423.3:p.Ser264Leu
NM_005921.1:c.791C>T	NP_005912.1:p.Ser264Leu
XM_005248519.3:c.413C>T	XP_005248576.2:p.Ser138Leu
XM_011543406.1:c.536C>T	XP_011541708.1:p.Ser179Leu
XM_011543407.1:c.791C>T	XP_011541709.1:p.Ser264Leu
XM_011543408.1:c.791C>T	XP_011541710.1:p.Ser264Leu
XM_017009484.1:c.380C>T	XP_016864973.1:p.Ser127Leu
XM_017009485.1:c.302C>T	XP_016864974.1:p.Ser101Leu
XR_001742068.2:n.822C>T
NM_005921.2:c.791C>T MANE Select	NP_005912.1:p.Ser264Leu