Canonical Allele Identifier: CA557870083

Gene: DNAH5

Linked Data

• gnomAD v2: 5-13769376-A-ATTT
• gnomAD v3: 5-13769267-A-ATTT
• gnomAD v4: 5-13769267-A-ATTT
• MyVariant Identifiers: chr5:g.13769376_13769377insTTT (hg19) ; chr5:g.13769267_13769268insTTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13769267_13769268insTTT , CM000667.2:g.13769267_13769268insTTT	GRCh38
NC_000005.9:g.13769376_13769377insTTT , CM000667.1:g.13769376_13769377insTTT	GRCh37
NC_000005.8:g.13822376_13822377insTTT	NCBI36
NG_013081.1:g.180213_180214insAAA
NG_013081.2:g.180213_180214insAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9721-132_9721-131insAAA MANE Select	ENSP00000265104.4:n.9721-132_9721-131insAAA
ENST00000681290.1:c.9676-132_9676-131insAAA	ENSP00000505288.1:n.9676-132_9676-131insAAA
ENST00000265104.4:c.9721-132_9721-131insAAA	ENSP00000265104.4:n.9721-132_9721-131insAAA
ENST00000504001.3:n.433-132_433-131insAAA
NM_001369.2:c.9721-132_9721-131insAAA	NP_001360.1:n.9721-132_9721-131insAAA
XM_005248262.2:c.9676-132_9676-131insAAA	XP_005248319.1:n.9676-132_9676-131insAAA
XM_005248262.3:c.9829-132_9829-131insAAA	XP_005248319.2:n.9829-132_9829-131insAAA
XM_017009177.1:c.9829-132_9829-131insAAA	XP_016864666.1:n.9829-132_9829-131insAAA
XM_017009178.1:c.8734-132_8734-131insAAA	XP_016864667.1:n.8734-132_8734-131insAAA
XM_017009179.2:c.8734-132_8734-131insAAA	XP_016864668.1:n.8734-132_8734-131insAAA
XM_017009180.1:c.9829-132_9829-131insAAA	XP_016864669.1:n.9829-132_9829-131insAAA
XM_017009181.1:c.9829-132_9829-131insAAA	XP_016864670.1:n.9829-132_9829-131insAAA
XM_017009182.1:c.9829-132_9829-131insAAA	XP_016864671.1:n.9829-132_9829-131insAAA
XM_017009185.1:c.4918-132_4918-131insAAA	XP_016864674.1:n.4918-132_4918-131insAAA
XM_017009186.1:c.4471-132_4471-131insAAA	XP_016864675.1:n.4471-132_4471-131insAAA
XM_017009188.1:c.3808-132_3808-131insAAA	XP_016864677.1:n.3808-132_3808-131insAAA
XM_024454388.1:c.8734-132_8734-131insAAA	XP_024310156.1:n.8734-132_8734-131insAAA
XM_024454389.1:c.8323-132_8323-131insAAA	XP_024310157.1:n.8323-132_8323-131insAAA
NM_001369.3:c.9721-132_9721-131insAAA MANE Select	NP_001360.1:n.9721-132_9721-131insAAA