Canonical Allele Identifier: CA13959808

Gene: BMP4

Linked Data

• dbSNP Id: rs2855530
• gnomAD v2: 14-54421917-G-C
• gnomAD v3: 14-53955199-G-C
• gnomAD v4: 14-53955199-G-C
• MyVariant Identifiers: chr14:g.54421917G>C (hg19) ; chr14:g.53955199G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.53955199G>C , CM000676.2:g.53955199G>C	GRCh38
NC_000014.8:g.54421917G>C , CM000676.1:g.54421917G>C	GRCh37
NC_000014.7:g.53491667G>C	NCBI36
NG_009215.1:g.6638C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000245451.9:c.-133+1351C>G MANE Select	ENSP00000245451.4:n.-133+1351C>G
ENST00000245451.8:c.-133+1351C>G	ENSP00000245451.4:n.-133+1351C>G
ENST00000559087.5:c.-133+1560C>G	ENSP00000453485.1:n.-133+1560C>G
ENST00000559642.1:c.-132-1799C>G	ENSP00000453467.1:n.-132-1799C>G
NM_001202.3:c.-133+1351C>G	NP_001193.2:n.-133+1351C>G
NM_130850.2:c.-133+1560C>G	NP_570911.2:n.-133+1560C>G
NM_001202.5:c.-133+1351C>G	NP_001193.2:n.-133+1351C>G
NM_001347912.1:c.62+1560C>G	NP_001334841.1:n.62+1560C>G
NM_001347913.1:c.-269+1351C>G	NP_001334842.1:n.-269+1351C>G
NM_130850.4:c.-133+1560C>G	NP_570911.2:n.-133+1560C>G
NM_001202.6:c.-133+1351C>G MANE Select	NP_001193.2:n.-133+1351C>G
NM_130850.5:c.-133+1560C>G	NP_570911.2:n.-133+1560C>G
NM_001347913.2:c.-269+1351C>G	NP_001334842.1:n.-269+1351C>G