Canonical Allele Identifier: CA291084394
Gene: MAP3K14 HGNC NCBI

Linked Data

dbSNP Id: rs567532658
gnomAD v3: 17-45306172-C-T
gnomAD v4: 17-45306172-C-T
MyVariant Identifiers: chr17:g.43383538C>T (hg19) chr17:g.45306172C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.45306172C>T , CM000679.2:g.45306172C>T GRCh38
NC_000017.10:g.43383538C>T , CM000679.1:g.43383538C>T GRCh37
NC_000017.9:g.40739321C>T NCBI36
NG_033823.1:g.15877G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000344686.8:c.-21+10788G>A MANE Select ENSP00000478552.1:n.-21+10788G>A
ENST00000617331.3:c.-21+6113G>A ENSP00000480974.3:n.-21+6113G>A
ENST00000344686.6:c.-21+10788G>A ENSP00000478552.1:n.-21+10788G>A
ENST00000617331.1:c.-21+10788G>A ENSP00000480974.1:n.-21+10788G>A
NM_003954.4:c.-21+10788G>A NP_003945.2:n.-21+10788G>A
XM_011525441.1:c.-21+6113G>A XP_011523743.1:n.-21+6113G>A
XR_934591.1:n.89+10788G>A
NM_003954.5:c.-21+10788G>A MANE Select NP_003945.2:n.-21+10788G>A
XM_011525441.2:c.-21+6113G>A XP_011523743.1:n.-21+6113G>A
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