Canonical Allele Identifier: CA15384493
Gene: MAP3K1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56832039G>A , CM000667.2:g.56832039G>A GRCh38
NC_000005.9:g.56127866G>A , CM000667.1:g.56127866G>A GRCh37
NC_000005.8:g.56163623G>A NCBI36
NG_031884.1:g.21967G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.482+15984G>A MANE Select ENSP00000382423.3:n.482+15984G>A
ENST00000399503.3:c.482+15984G>A ENSP00000382423.3:n.482+15984G>A
NM_005921.1:c.482+15984G>A NP_005912.1:n.482+15984G>A
XM_005248519.3:c.104+11223G>A XP_005248576.2:n.104+11223G>A
XM_011543406.1:c.227+15704G>A XP_011541708.1:n.227+15704G>A
XM_011543407.1:c.482+15984G>A XP_011541709.1:n.482+15984G>A
XM_011543408.1:c.482+15984G>A XP_011541710.1:n.482+15984G>A
XM_017009484.1:c.71+11223G>A XP_016864973.1:n.71+11223G>A
XM_017009485.1:c.-8+14923G>A XP_016864974.1:n.-8+14923G>A
XR_001742068.2:n.513+15984G>A
NM_005921.2:c.482+15984G>A MANE Select NP_005912.1:n.482+15984G>A
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