Canonical Allele Identifier: CA1226700558

Gene: CAPN9

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230787316C= , CM000663.2:g.230787316C=	GRCh38
NC_000001.10:g.230923062C= , CM000663.1:g.230923062C=	GRCh37
NC_000001.9:g.228989685C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271971.7:c.1519-206C= MANE Select	ENSP00000271971.2:n.1519-206C=
ENST00000271971.6:c.1519-206C=	ENSP00000271971.2:n.1519-206C=
ENST00000354537.1:c.1441-206C=	ENSP00000346538.1:n.1441-206C=
ENST00000366666.6:c.1330-206C=	ENSP00000355626.2:n.1330-206C=
NM_006615.2:c.1519-206C=	NP_006606.1:n.1519-206C=
NM_016452.1:c.1441-206C=	NP_057536.1:n.1441-206C=
XM_005273010.2:c.1330-206C=	XP_005273067.1:n.1330-206C=
XM_011544017.1:c.1519-206C=	XP_011542319.1:n.1519-206C=
XM_011544018.1:c.1441-206C=	XP_011542320.1:n.1441-206C=
XM_011544019.1:c.1330-206C=	XP_011542321.1:n.1330-206C=
XM_011544020.1:c.934-206C=	XP_011542322.1:n.934-206C=
XR_949127.1:n.1734-206C=
NM_001319676.1:c.1330-206C=	NP_001306605.1:n.1330-206C=
NM_016452.2:c.1441-206C=	NP_057536.1:n.1441-206C=
XM_011544019.2:c.1330-206C=	XP_011542321.1:n.1330-206C=
XM_017000098.1:c.1435-206C=	XP_016855587.1:n.1435-206C=
XM_017000099.1:c.934-206C=	XP_016855588.1:n.934-206C=
XM_024452513.1:c.565-206C=	XP_024308281.1:n.565-206C=
XM_024452514.1:c.565-206C=	XP_024308282.1:n.565-206C=
XR_001736933.1:n.1616-206C=
XR_001738518.1:n.84+7797G=
NM_006615.3:c.1519-206C= MANE Select	NP_006606.1:n.1519-206C=
NM_001319676.2:c.1330-206C=	NP_001306605.1:n.1330-206C=
NM_016452.3:c.1441-206C=	NP_057536.1:n.1441-206C=