Canonical Allele Identifier: CA1470731566
Gene: BMP2K HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78865785T= , CM000666.2:g.78865785T= GRCh38
NC_000004.11:g.79786939T= , CM000666.1:g.79786939T= GRCh37
NC_000004.10:g.80005963T= NCBI36
NG_047162.1:g.94408T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000502613.3:c.1231+65T= MANE Select ENSP00000424668.2:n.1231+65T=
ENST00000335016.9:c.1231+65T= ENSP00000334836.5:n.1231+65T=
ENST00000389010.7:c.*207+65T= ENSP00000373662.3:n.*207+65T=
ENST00000502613.1:c.308+65T=
ENST00000502871.5:c.1231+65T= ENSP00000421768.1:n.1231+65T=
ENST00000628286.1:c.*207+65T= ENSP00000487317.1:n.*207+65T=
NM_017593.3:c.1231+65T= NP_060063.2:n.1231+65T=
NM_198892.1:c.1231+65T= NP_942595.1:n.1231+65T=
XM_005263117.1:c.1231+65T= XP_005263174.1:n.1231+65T=
XM_011532101.1:c.991+65T= XP_011530403.1:n.991+65T=
XM_011532102.1:c.1231+65T= XP_011530404.1:n.1231+65T=
XM_017008381.1:c.991+65T= XP_016863870.1:n.991+65T=
XM_017008382.1:c.343+65T= XP_016863871.1:n.343+65T=
NM_017593.4:c.1231+65T= NP_060063.2:n.1231+65T=
NM_017593.5:c.1231+65T= NP_060063.2:n.1231+65T=
NM_198892.2:c.1231+65T= MANE Select NP_942595.1:n.1231+65T=