Canonical Allele Identifier: CA1226700475

Gene: CAPN9

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230787128_230787133delinsACTCTT , CM000663.2:g.230787128_230787133delinsACTCTT	GRCh38
NC_000001.10:g.230922874_230922879delinsACTCTT , CM000663.1:g.230922874_230922879delinsACTCTT	GRCh37
NC_000001.9:g.228989497_228989502delinsACTCTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271971.7:c.1519-394_1519-389delinsACTCTT MANE Select	ENSP00000271971.2:n.1519-394_1519-389delinsACTCTT
ENST00000271971.6:c.1519-394_1519-389delinsACTCTT	ENSP00000271971.2:n.1519-394_1519-389delinsACTCTT
ENST00000354537.1:c.1441-394_1441-389delinsACTCTT	ENSP00000346538.1:n.1441-394_1441-389delinsACTCTT
ENST00000366666.6:c.1330-394_1330-389delinsACTCTT	ENSP00000355626.2:n.1330-394_1330-389delinsACTCTT
NM_006615.2:c.1519-394_1519-389delinsACTCTT	NP_006606.1:n.1519-394_1519-389delinsACTCTT
NM_016452.1:c.1441-394_1441-389delinsACTCTT	NP_057536.1:n.1441-394_1441-389delinsACTCTT
XM_005273010.2:c.1330-394_1330-389delinsACTCTT	XP_005273067.1:n.1330-394_1330-389delinsACTCTT
XM_011544017.1:c.1519-394_1519-389delinsACTCTT	XP_011542319.1:n.1519-394_1519-389delinsACTCTT
XM_011544018.1:c.1441-394_1441-389delinsACTCTT	XP_011542320.1:n.1441-394_1441-389delinsACTCTT
XM_011544019.1:c.1330-394_1330-389delinsACTCTT	XP_011542321.1:n.1330-394_1330-389delinsACTCTT
XM_011544020.1:c.934-394_934-389delinsACTCTT	XP_011542322.1:n.934-394_934-389delinsACTCTT
XR_949127.1:n.1734-394_1734-389delinsACTCTT
NM_001319676.1:c.1330-394_1330-389delinsACTCTT	NP_001306605.1:n.1330-394_1330-389delinsACTCTT
NM_016452.2:c.1441-394_1441-389delinsACTCTT	NP_057536.1:n.1441-394_1441-389delinsACTCTT
XM_011544019.2:c.1330-394_1330-389delinsACTCTT	XP_011542321.1:n.1330-394_1330-389delinsACTCTT
XM_017000098.1:c.1435-394_1435-389delinsACTCTT	XP_016855587.1:n.1435-394_1435-389delinsACTCTT
XM_017000099.1:c.934-394_934-389delinsACTCTT	XP_016855588.1:n.934-394_934-389delinsACTCTT
XM_024452513.1:c.565-394_565-389delinsACTCTT	XP_024308281.1:n.565-394_565-389delinsACTCTT
XM_024452514.1:c.565-394_565-389delinsACTCTT	XP_024308282.1:n.565-394_565-389delinsACTCTT
XR_001736933.1:n.1616-394_1616-389delinsACTCTT
XR_001738518.1:n.84+7980_84+7985delinsAAGAGT
NM_006615.3:c.1519-394_1519-389delinsACTCTT MANE Select	NP_006606.1:n.1519-394_1519-389delinsACTCTT
NM_001319676.2:c.1330-394_1330-389delinsACTCTT	NP_001306605.1:n.1330-394_1330-389delinsACTCTT
NM_016452.3:c.1441-394_1441-389delinsACTCTT	NP_057536.1:n.1441-394_1441-389delinsACTCTT