Canonical Allele Identifier: CA2661559164

Gene: ACVR1

Linked Data

• gnomAD v4: 2-157770307-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.157770310del , CM000664.2:g.157770310del	GRCh38
NC_000002.11:g.158626822del , CM000664.1:g.158626822del	GRCh37
NC_000002.10:g.158335068del	NCBI36
NG_008004.1:g.109804del

Transcript Alleles

HGVS	Amino-acid change
ENST00000682025.1:c.790+60del	ENSP00000507086.1:n.790+60del
ENST00000682300.1:c.790+60del	ENSP00000507102.1:n.790+60del
ENST00000682690.1:n.807+60del
ENST00000683404.1:c.790+60del	ENSP00000506824.1:n.790+60del
ENST00000683426.1:c.790+60del	ENSP00000507597.1:n.790+60del
ENST00000683441.1:c.790+60del	ENSP00000508189.1:n.790+60del
ENST00000683487.1:c.790+60del	ENSP00000507113.1:n.790+60del
ENST00000683820.1:c.790+60del	ENSP00000507727.1:n.790+60del
ENST00000684104.1:n.998+60del
ENST00000684348.1:c.790+60del	ENSP00000508136.1:n.790+60del
ENST00000684595.1:c.790+60del	ENSP00000507730.1:n.790+60del
ENST00000424669.6:c.790+60del	ENSP00000400767.2:n.790+60del
ENST00000434821.7:c.790+60del MANE Select	ENSP00000405004.1:n.790+60del
ENST00000539637.6:c.790+60del	ENSP00000440091.2:n.790+60del
ENST00000672582.1:c.790+60del	ENSP00000500605.1:n.790+60del
ENST00000673324.1:c.790+60del	ENSP00000500109.1:n.790+60del
ENST00000263640.7:c.790+60del	ENSP00000263640.3:n.790+60del
ENST00000409283.6:c.790+60del	ENSP00000387273.2:n.790+60del
ENST00000410057.6:c.790+60del	ENSP00000387127.2:n.790+60del
ENST00000434821.5:c.790+60del	ENSP00000405004.1:n.790+60del
NM_001105.4:c.790+60del	NP_001096.1:n.790+60del
NM_001111067.2:c.790+60del	NP_001104537.1:n.790+60del
XM_005246939.2:c.790+60del	XP_005246996.1:n.790+60del
XM_005246940.2:c.790+60del	XP_005246997.1:n.790+60del
XM_006712825.2:c.790+60del	XP_006712888.1:n.790+60del
XM_011512106.1:c.790+60del	XP_011510408.1:n.790+60del
XM_011512107.1:c.790+60del	XP_011510409.1:n.790+60del
XM_011512108.1:c.790+60del	XP_011510410.1:n.790+60del
NM_001347663.1:c.790+60del	NP_001334592.1:n.790+60del
NM_001347664.1:c.790+60del	NP_001334593.1:n.790+60del
NM_001347665.1:c.790+60del	NP_001334594.1:n.790+60del
NM_001347666.1:c.790+60del	NP_001334595.1:n.790+60del
NM_001347667.1:c.790+60del	NP_001334596.1:n.790+60del
XM_006712825.4:c.790+60del	XP_006712888.1:n.790+60del
XM_011512108.3:c.790+60del	XP_011510410.1:n.790+60del
NM_001105.5:c.790+60del	NP_001096.1:n.790+60del
NM_001111067.4:c.790+60del MANE Select	NP_001104537.1:n.790+60del
NM_001347667.2:c.790+60del	NP_001334596.1:n.790+60del