Canonical Allele Identifier: CA2261795572
Gene: MAP3K14 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.45306019T= , CM000679.2:g.45306019T= GRCh38
NC_000017.10:g.43383385T= , CM000679.1:g.43383385T= GRCh37
NC_000017.9:g.40739168T= NCBI36
NG_033823.1:g.16030A=

Transcript Alleles

HGVS Amino-acid change
ENST00000344686.8:c.-21+10941A= MANE Select ENSP00000478552.1:n.-21+10941A=
ENST00000617331.3:c.-21+6266A= ENSP00000480974.3:n.-21+6266A=
ENST00000344686.6:c.-21+10941A= ENSP00000478552.1:n.-21+10941A=
ENST00000617331.1:c.-21+10941A= ENSP00000480974.1:n.-21+10941A=
NM_003954.4:c.-21+10941A= NP_003945.2:n.-21+10941A=
XM_011525441.1:c.-21+6266A= XP_011523743.1:n.-21+6266A=
XR_934591.1:n.89+10941A=
NM_003954.5:c.-21+10941A= MANE Select NP_003945.2:n.-21+10941A=
XM_011525441.2:c.-21+6266A= XP_011523743.1:n.-21+6266A=
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