Canonical Allele Identifier: CA557862793

Gene: DNAH5

Linked Data

• dbSNP Id: rs1320336179
• gnomAD v2: 5-13708489-A-C
• gnomAD v4: 5-13708380-A-C
• MyVariant Identifiers: chr5:g.13708489A>C (hg19) ; chr5:g.13708380A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13708380A>C , CM000667.2:g.13708380A>C	GRCh38
NC_000005.9:g.13708489A>C , CM000667.1:g.13708489A>C	GRCh37
NC_000005.8:g.13761489A>C	NCBI36
NG_013081.1:g.241101T>G
NG_013081.2:g.241101T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683611.1:n.459-45T>G
ENST00000265104.5:c.13126-45T>G MANE Select	ENSP00000265104.4:n.13126-45T>G
ENST00000681290.1:c.13081-45T>G	ENSP00000505288.1:n.13081-45T>G
ENST00000265104.4:c.13126-45T>G	ENSP00000265104.4:n.13126-45T>G
NM_001369.2:c.13126-45T>G	NP_001360.1:n.13126-45T>G
XM_005248262.2:c.13081-45T>G	XP_005248319.1:n.13081-45T>G
XM_005248262.3:c.13234-45T>G	XP_005248319.2:n.13234-45T>G
XM_017009177.1:c.12814-45T>G	XP_016864666.1:n.12814-45T>G
XM_017009178.1:c.12139-45T>G	XP_016864667.1:n.12139-45T>G
XM_017009179.2:c.12139-45T>G	XP_016864668.1:n.12139-45T>G
XM_017009185.1:c.8323-45T>G	XP_016864674.1:n.8323-45T>G
XM_017009186.1:c.7876-45T>G	XP_016864675.1:n.7876-45T>G
XM_017009188.1:c.7213-45T>G	XP_016864677.1:n.7213-45T>G
XM_024454388.1:c.12139-45T>G	XP_024310156.1:n.12139-45T>G
XM_024454389.1:c.11728-45T>G	XP_024310157.1:n.11728-45T>G
NM_001369.3:c.13126-45T>G MANE Select	NP_001360.1:n.13126-45T>G