Canonical Allele Identifier: CA2708944222
Gene: MAP3K1 HGNC NCBI

Linked Data

dbSNP Id: rs2111874813

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56859920G>A , CM000667.2:g.56859920G>A GRCh38
NC_000005.9:g.56155747G>A , CM000667.1:g.56155747G>A GRCh37
NC_000005.8:g.56191504G>A NCBI36
NG_031884.1:g.49848G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.834+5G>A MANE Select ENSP00000382423.3:n.834+5G>A
ENST00000399503.3:c.834+5G>A ENSP00000382423.3:n.834+5G>A
NM_005921.1:c.834+5G>A NP_005912.1:n.834+5G>A
XM_005248519.3:c.456+5G>A XP_005248576.2:n.456+5G>A
XM_011543406.1:c.579+5G>A XP_011541708.1:n.579+5G>A
XM_011543407.1:c.834+5G>A XP_011541709.1:n.834+5G>A
XM_011543408.1:c.834+5G>A XP_011541710.1:n.834+5G>A
XM_017009484.1:c.423+5G>A XP_016864973.1:n.423+5G>A
XM_017009485.1:c.345+5G>A XP_016864974.1:n.345+5G>A
XR_001742068.2:n.865+5G>A
NM_005921.2:c.834+5G>A MANE Select NP_005912.1:n.834+5G>A