Canonical Allele Identifier: CA59255804

Gene: ACVR1C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.157543065G>A , CM000664.2:g.157543065G>A	GRCh38
NC_000002.11:g.158399577G>A , CM000664.1:g.158399577G>A	GRCh37
NC_000002.10:g.158107823G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243349.13:c.944-203C>T MANE Select	ENSP00000243349.7:n.944-203C>T
ENST00000243349.12:c.944-203C>T	ENSP00000243349.7:n.944-203C>T
ENST00000335450.7:c.704-203C>T	ENSP00000335178.7:n.704-203C>T
ENST00000348328.9:c.473-203C>T	ENSP00000335139.6:n.473-203C>T
ENST00000409680.7:c.794-203C>T	ENSP00000387168.3:n.794-203C>T
NM_001111031.1:c.794-203C>T	NP_001104501.1:n.794-203C>T
NM_001111032.1:c.704-203C>T	NP_001104502.1:n.704-203C>T
NM_001111033.1:c.473-203C>T	NP_001104503.1:n.473-203C>T
NM_145259.2:c.944-203C>T	NP_660302.2:n.944-203C>T
NM_145259.3:c.944-203C>T MANE Select	NP_660302.2:n.944-203C>T
NM_001111032.2:c.704-203C>T	NP_001104502.1:n.704-203C>T
NM_001111033.2:c.473-203C>T	NP_001104503.1:n.473-203C>T
NM_001111031.2:c.794-203C>T	NP_001104501.1:n.794-203C>T