Canonical Allele Identifier: CA384900071

Gene: ACVRL1

Linked Data

• MyVariant Identifiers: chr12:g.52308283A>C (hg19) ; chr12:g.51914499A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51914499A>C , CM000674.2:g.51914499A>C	GRCh38
NC_000012.11:g.52308283A>C , CM000674.1:g.52308283A>C	GRCh37
NC_000012.10:g.50594550A>C	NCBI36
NG_009549.1:g.12082A>C , LRG_543:g.12082A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000547400.6:c.416A>C	ENSP00000446724.2:p.Lys139Thr
ENST00000551576.6:c.686A>C	ENSP00000455848.2:p.Lys229Thr
ENST00000552678.2:c.686A>C	ENSP00000457394.2:p.Lys229Thr
ENST00000388922.9:c.686A>C MANE Select	ENSP00000373574.4:p.Lys229Thr
ENST00000388922.8:c.686A>C	ENSP00000373574.4:p.Lys229Thr
ENST00000419526.6:c.164A>C	ENSP00000392492.2:p.Lys55Thr
ENST00000547400.5:c.416A>C	ENSP00000446724.1:p.Lys139Thr
ENST00000550683.5:c.728A>C	ENSP00000447884.1:p.Lys243Thr
NM_000020.2:c.686A>C , LRG_543t1:c.686A>C	NP_000011.2:p.Lys229Thr
NM_001077401.1:c.686A>C	NP_001070869.1:p.Lys229Thr
XM_005269235.2:c.686A>C	XP_005269292.1:p.Lys229Thr
XM_011539008.1:c.416A>C	XP_011537310.1:p.Lys139Thr
XM_024449279.1:c.-104A>C	XP_024305047.1:n.-104A>C
NM_000020.3:c.686A>C MANE Select	NP_000011.2:p.Lys229Thr
NM_001077401.2:c.686A>C	NP_001070869.1:p.Lys229Thr