Canonical Allele Identifier: CA359786153

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177632A>C (hg19) ; chr5:g.56881805A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881805A>C , CM000667.2:g.56881805A>C	GRCh38
NC_000005.9:g.56177632A>C , CM000667.1:g.56177632A>C	GRCh37
NC_000005.8:g.56213389A>C	NCBI36
NG_031884.1:g.71733A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2605A>C MANE Select	ENSP00000382423.3:p.Ile869Leu
ENST00000399503.3:c.2605A>C	ENSP00000382423.3:p.Ile869Leu
NM_005921.1:c.2605A>C	NP_005912.1:p.Ile869Leu
XM_005248519.3:c.2227A>C	XP_005248576.2:p.Ile743Leu
XM_011543406.1:c.2350A>C	XP_011541708.1:p.Ile784Leu
XM_011543407.1:c.2326A>C	XP_011541709.1:p.Ile776Leu
XM_011543408.1:c.2605A>C	XP_011541710.1:p.Ile869Leu
XM_017009484.1:c.2194A>C	XP_016864973.1:p.Ile732Leu
XM_017009485.1:c.2116A>C	XP_016864974.1:p.Ile706Leu
XR_001742068.2:n.2636A>C
NM_005921.2:c.2605A>C MANE Select	NP_005912.1:p.Ile869Leu