Canonical Allele Identifier: CA2671157192
Gene: BMP2K HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78865821_78865822insT , CM000666.2:g.78865821_78865822insT GRCh38
NC_000004.11:g.79786975_79786976insT , CM000666.1:g.79786975_79786976insT GRCh37
NC_000004.10:g.80005999_80006000insT NCBI36
NG_047162.1:g.94444_94445insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000502613.3:c.1231+101_1231+102insT MANE Select ENSP00000424668.2:n.1231+101_1231+102insT
ENST00000335016.9:c.1231+101_1231+102insT ENSP00000334836.5:n.1231+101_1231+102insT
ENST00000389010.7:c.*207+101_*207+102insT ENSP00000373662.3:n.*207+101_*207+102insT
ENST00000502613.1:c.308+101_308+102insT
ENST00000502871.5:c.1231+101_1231+102insT ENSP00000421768.1:n.1231+101_1231+102insT
ENST00000628286.1:c.*207+101_*207+102insT ENSP00000487317.1:n.*207+101_*207+102insT
NM_017593.3:c.1231+101_1231+102insT NP_060063.2:n.1231+101_1231+102insT
NM_198892.1:c.1231+101_1231+102insT NP_942595.1:n.1231+101_1231+102insT
XM_005263117.1:c.1231+101_1231+102insT XP_005263174.1:n.1231+101_1231+102insT
XM_011532101.1:c.991+101_991+102insT XP_011530403.1:n.991+101_991+102insT
XM_011532102.1:c.1231+101_1231+102insT XP_011530404.1:n.1231+101_1231+102insT
XM_017008381.1:c.991+101_991+102insT XP_016863870.1:n.991+101_991+102insT
XM_017008382.1:c.343+101_343+102insT XP_016863871.1:n.343+101_343+102insT
NM_017593.4:c.1231+101_1231+102insT NP_060063.2:n.1231+101_1231+102insT
NM_017593.5:c.1231+101_1231+102insT NP_060063.2:n.1231+101_1231+102insT
NM_198892.2:c.1231+101_1231+102insT MANE Select NP_942595.1:n.1231+101_1231+102insT