Canonical Allele Identifier: CA357378658

Gene: BMP2K

Linked Data

• MyVariant Identifiers: chr4:g.79786836T>A (hg19) ; chr4:g.78865682T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78865682T>A , CM000666.2:g.78865682T>A	GRCh38
NC_000004.11:g.79786836T>A , CM000666.1:g.79786836T>A	GRCh37
NC_000004.10:g.80005860T>A	NCBI36
NG_047162.1:g.94305T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502613.3:c.1193T>A MANE Select	ENSP00000424668.2:p.Val398Asp
ENST00000335016.9:c.1193T>A	ENSP00000334836.5:p.Val398Asp
ENST00000389010.7:c.*169T>A	ENSP00000373662.3:n.*169T>A
ENST00000502613.1:c.270T>A
ENST00000502871.5:c.1193T>A	ENSP00000421768.1:p.Val398Asp
ENST00000505725.1:n.475T>A
ENST00000628286.1:c.*169T>A	ENSP00000487317.1:n.*169T>A
NM_017593.3:c.1193T>A	NP_060063.2:p.Val398Asp
NM_198892.1:c.1193T>A	NP_942595.1:p.Val398Asp
XM_005263117.1:c.1193T>A	XP_005263174.1:p.Val398Asp
XM_011532101.1:c.953T>A	XP_011530403.1:p.Val318Asp
XM_011532102.1:c.1193T>A	XP_011530404.1:p.Val398Asp
XM_017008381.1:c.953T>A	XP_016863870.1:p.Val318Asp
XM_017008382.1:c.305T>A	XP_016863871.1:p.Val102Asp
NM_017593.4:c.1193T>A	NP_060063.2:p.Val398Asp
NM_017593.5:c.1193T>A	NP_060063.2:p.Val398Asp
NM_198892.2:c.1193T>A MANE Select	NP_942595.1:p.Val398Asp