Canonical Allele Identifier: CA439976580

Gene: BMP2K

Linked Data

• MyVariant Identifiers: chr4:g.79786807C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78865653C>T , CM000666.2:g.78865653C>T	GRCh38
NC_000004.11:g.79786807C>T , CM000666.1:g.79786807C>T	GRCh37
NC_000004.10:g.80005831C>T	NCBI36
NG_047162.1:g.94276C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502613.3:c.1164C>T MANE Select	ENSP00000424668.2:p.Thr388=
ENST00000335016.9:c.1164C>T	ENSP00000334836.5:p.Thr388=
ENST00000389010.7:c.*140C>T	ENSP00000373662.3:n.*140C>T
ENST00000502613.1:c.241C>T
ENST00000502871.5:c.1164C>T	ENSP00000421768.1:p.Thr388=
ENST00000505725.1:n.446C>T
ENST00000628286.1:c.*140C>T	ENSP00000487317.1:n.*140C>T
NM_017593.3:c.1164C>T	NP_060063.2:p.Thr388=
NM_198892.1:c.1164C>T	NP_942595.1:p.Thr388=
XM_005263117.1:c.1164C>T	XP_005263174.1:p.Thr388=
XM_011532101.1:c.924C>T	XP_011530403.1:p.Thr308=
XM_011532102.1:c.1164C>T	XP_011530404.1:p.Thr388=
XM_017008381.1:c.924C>T	XP_016863870.1:p.Thr308=
XM_017008382.1:c.276C>T	XP_016863871.1:p.Thr92=
NM_017593.4:c.1164C>T	NP_060063.2:p.Thr388=
NM_017593.5:c.1164C>T	NP_060063.2:p.Thr388=
NM_198892.2:c.1164C>T MANE Select	NP_942595.1:p.Thr388=