Canonical Allele Identifier: CA2673269817

Gene: DNAH5

Linked Data

• gnomAD v4: 5-13769248-T-TTTTTTTTTTTTTTTTTTTTTG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13769265_13769266insTTTGTTTTTTTTTTTTTTTTT , CM000667.2:g.13769265_13769266insTTTGTTTTTTTTTTTTTTTTT	GRCh38
NC_000005.9:g.13769374_13769375insTTTGTTTTTTTTTTTTTTTTT , CM000667.1:g.13769374_13769375insTTTGTTTTTTTTTTTTTTTTT	GRCh37
NC_000005.8:g.13822374_13822375insTTTGTTTTTTTTTTTTTTTTT	NCBI36
NG_013081.1:g.180232_180233insCAAAAAAAAAAAAAAAAAAAA
NG_013081.2:g.180232_180233insCAAAAAAAAAAAAAAAAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9721-113_9721-112insCAAAAAAAAAAAAAAAAAAAA MANE Select	ENSP00000265104.4:n.9721-113_9721-112insCAAAAAAAAAAAAAAAAAAAA...
ENST00000681290.1:c.9676-113_9676-112insCAAAAAAAAAAAAAAAAAAAA	ENSP00000505288.1:n.9676-113_9676-112insCAAAAAAAAAAAAAAAAAAAA...
ENST00000265104.4:c.9721-113_9721-112insCAAAAAAAAAAAAAAAAAAAA	ENSP00000265104.4:n.9721-113_9721-112insCAAAAAAAAAAAAAAAAAAAA...
ENST00000504001.3:n.433-113_433-112insCAAAAAAAAAAAAAAAAAAAA
NM_001369.2:c.9721-113_9721-112insCAAAAAAAAAAAAAAAAAAAA	NP_001360.1:n.9721-113_9721-112insCAAAAAAAAAAAAAAAAAAAA
XM_005248262.2:c.9676-113_9676-112insCAAAAAAAAAAAAAAAAAAAA	XP_005248319.1:n.9676-113_9676-112insCAAAAAAAAAAAAAAAAAAAA
XM_005248262.3:c.9829-113_9829-112insCAAAAAAAAAAAAAAAAAAAA	XP_005248319.2:n.9829-113_9829-112insCAAAAAAAAAAAAAAAAAAAA
XM_017009177.1:c.9829-113_9829-112insCAAAAAAAAAAAAAAAAAAAA	XP_016864666.1:n.9829-113_9829-112insCAAAAAAAAAAAAAAAAAAAA
XM_017009178.1:c.8734-113_8734-112insCAAAAAAAAAAAAAAAAAAAA	XP_016864667.1:n.8734-113_8734-112insCAAAAAAAAAAAAAAAAAAAA
XM_017009179.2:c.8734-113_8734-112insCAAAAAAAAAAAAAAAAAAAA	XP_016864668.1:n.8734-113_8734-112insCAAAAAAAAAAAAAAAAAAAA
XM_017009180.1:c.9829-113_9829-112insCAAAAAAAAAAAAAAAAAAAA	XP_016864669.1:n.9829-113_9829-112insCAAAAAAAAAAAAAAAAAAAA
XM_017009181.1:c.9829-113_9829-112insCAAAAAAAAAAAAAAAAAAAA	XP_016864670.1:n.9829-113_9829-112insCAAAAAAAAAAAAAAAAAAAA
XM_017009182.1:c.9829-113_9829-112insCAAAAAAAAAAAAAAAAAAAA	XP_016864671.1:n.9829-113_9829-112insCAAAAAAAAAAAAAAAAAAAA
XM_017009185.1:c.4918-113_4918-112insCAAAAAAAAAAAAAAAAAAAA	XP_016864674.1:n.4918-113_4918-112insCAAAAAAAAAAAAAAAAAAAA
XM_017009186.1:c.4471-113_4471-112insCAAAAAAAAAAAAAAAAAAAA	XP_016864675.1:n.4471-113_4471-112insCAAAAAAAAAAAAAAAAAAAA
XM_017009188.1:c.3808-113_3808-112insCAAAAAAAAAAAAAAAAAAAA	XP_016864677.1:n.3808-113_3808-112insCAAAAAAAAAAAAAAAAAAAA
XM_024454388.1:c.8734-113_8734-112insCAAAAAAAAAAAAAAAAAAAA	XP_024310156.1:n.8734-113_8734-112insCAAAAAAAAAAAAAAAAAAAA
XM_024454389.1:c.8323-113_8323-112insCAAAAAAAAAAAAAAAAAAAA	XP_024310157.1:n.8323-113_8323-112insCAAAAAAAAAAAAAAAAAAAA
NM_001369.3:c.9721-113_9721-112insCAAAAAAAAAAAAAAAAAAAA MANE Select	NP_001360.1:n.9721-113_9721-112insCAAAAAAAAAAAAAAAAAAAA