Canonical Allele Identifier: CA389784694

Gene: BMP4

Linked Data

• gnomAD v4: 14-53950817-G-T
• MyVariant Identifiers: chr14:g.54417535G>T (hg19) ; chr14:g.53950817G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.53950817G>T , CM000676.2:g.53950817G>T	GRCh38
NC_000014.8:g.54417535G>T , CM000676.1:g.54417535G>T	GRCh37
NC_000014.7:g.53487285G>T	NCBI36
NG_009215.1:g.11020C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000245451.9:c.442C>A MANE Select	ENSP00000245451.4:p.Pro148Thr
ENST00000245451.8:c.442C>A	ENSP00000245451.4:p.Pro148Thr
ENST00000417573.5:c.442C>A	ENSP00000394165.1:p.Pro148Thr
ENST00000558961.1:c.300C>A	ENSP00000453691.1:p.Ser100=
ENST00000558984.1:c.442C>A	ENSP00000454134.1:p.Pro148Thr
ENST00000559087.5:c.442C>A	ENSP00000453485.1:p.Pro148Thr
ENST00000559501.1:c.253C>A	ENSP00000453365.1:p.Pro85Thr
NM_001202.3:c.442C>A	NP_001193.2:p.Pro148Thr
NM_130850.2:c.442C>A	NP_570911.2:p.Pro148Thr
NM_130851.2:c.442C>A	NP_570912.2:p.Pro148Thr
XM_005268015.3:c.442C>A	XP_005268072.1:p.Pro148Thr
NM_001202.5:c.442C>A	NP_001193.2:p.Pro148Thr
NM_001347912.1:c.583C>A	NP_001334841.1:p.Pro195Thr
NM_001347913.1:c.253C>A	NP_001334842.1:p.Pro85Thr
NM_001347914.1:c.442C>A	NP_001334843.1:p.Pro148Thr
NM_001347915.1:c.253C>A	NP_001334844.1:p.Pro85Thr
NM_001347916.1:c.442C>A	NP_001334845.1:p.Pro148Thr
NM_001347917.1:c.253C>A	NP_001334846.1:p.Pro85Thr
NM_130850.4:c.442C>A	NP_570911.2:p.Pro148Thr
NM_130851.3:c.442C>A	NP_570912.2:p.Pro148Thr
NM_001202.6:c.442C>A MANE Select	NP_001193.2:p.Pro148Thr
NM_130850.5:c.442C>A	NP_570911.2:p.Pro148Thr
NM_001347913.2:c.253C>A	NP_001334842.1:p.Pro85Thr
NM_001347914.2:c.442C>A	NP_001334843.1:p.Pro148Thr
NM_001347915.2:c.253C>A	NP_001334844.1:p.Pro85Thr
NM_130851.4:c.442C>A	NP_570912.2:p.Pro148Thr