Canonical Allele Identifier: CA984072812
Gene: MAP3K14 HGNC NCBI

Linked Data

gnomAD v3: 17-45306135-A-T
gnomAD v4: 17-45306135-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.45306135A>T , CM000679.2:g.45306135A>T GRCh38
NC_000017.10:g.43383501A>T , CM000679.1:g.43383501A>T GRCh37
NC_000017.9:g.40739284A>T NCBI36
NG_033823.1:g.15914T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000344686.8:c.-21+10825T>A MANE Select ENSP00000478552.1:n.-21+10825T>A
ENST00000617331.3:c.-21+6150T>A ENSP00000480974.3:n.-21+6150T>A
ENST00000344686.6:c.-21+10825T>A ENSP00000478552.1:n.-21+10825T>A
ENST00000617331.1:c.-21+10825T>A ENSP00000480974.1:n.-21+10825T>A
NM_003954.4:c.-21+10825T>A NP_003945.2:n.-21+10825T>A
XM_011525441.1:c.-21+6150T>A XP_011523743.1:n.-21+6150T>A
XR_934591.1:n.89+10825T>A
NM_003954.5:c.-21+10825T>A MANE Select NP_003945.2:n.-21+10825T>A
XM_011525441.2:c.-21+6150T>A XP_011523743.1:n.-21+6150T>A
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