Canonical Allele Identifier: CA1918833

Gene: ACVR1C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.157556366A>G , CM000664.2:g.157556366A>G	GRCh38
NC_000002.11:g.158412878A>G , CM000664.1:g.158412878A>G	GRCh37
NC_000002.10:g.158121124A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243349.13:c.305-34T>C MANE Select	ENSP00000243349.7:n.305-34T>C
ENST00000243349.12:c.305-34T>C	ENSP00000243349.7:n.305-34T>C
ENST00000335450.7:c.305-5974T>C	ENSP00000335178.7:n.305-5974T>C
ENST00000348328.9:c.305-11754T>C	ENSP00000335139.6:n.305-11754T>C
ENST00000409680.7:c.155-34T>C	ENSP00000387168.3:n.155-34T>C
NM_001111031.1:c.155-34T>C	NP_001104501.1:n.155-34T>C
NM_001111032.1:c.305-5974T>C	NP_001104502.1:n.305-5974T>C
NM_001111033.1:c.305-11754T>C	NP_001104503.1:n.305-11754T>C
NM_145259.2:c.305-34T>C	NP_660302.2:n.305-34T>C
NM_145259.3:c.305-34T>C MANE Select	NP_660302.2:n.305-34T>C
NM_001111032.2:c.305-5974T>C	NP_001104502.1:n.305-5974T>C
NM_001111033.2:c.305-11754T>C	NP_001104503.1:n.305-11754T>C
NM_001111031.2:c.155-34T>C	NP_001104501.1:n.155-34T>C