Canonical Allele Identifier: CA557862792

Gene: DNAH5

Linked Data

• dbSNP Id: rs1465673074
• gnomAD v2: 5-13708465-G-T
• gnomAD v4: 5-13708356-G-T
• MyVariant Identifiers: chr5:g.13708465G>T (hg19) ; chr5:g.13708356G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13708356G>T , CM000667.2:g.13708356G>T	GRCh38
NC_000005.9:g.13708465G>T , CM000667.1:g.13708465G>T	GRCh37
NC_000005.8:g.13761465G>T	NCBI36
NG_013081.1:g.241125C>A
NG_013081.2:g.241125C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000683611.1:n.459-21C>A
ENST00000265104.5:c.13126-21C>A MANE Select	ENSP00000265104.4:n.13126-21C>A
ENST00000681290.1:c.13081-21C>A	ENSP00000505288.1:n.13081-21C>A
ENST00000265104.4:c.13126-21C>A	ENSP00000265104.4:n.13126-21C>A
NM_001369.2:c.13126-21C>A	NP_001360.1:n.13126-21C>A
XM_005248262.2:c.13081-21C>A	XP_005248319.1:n.13081-21C>A
XM_005248262.3:c.13234-21C>A	XP_005248319.2:n.13234-21C>A
XM_017009177.1:c.12814-21C>A	XP_016864666.1:n.12814-21C>A
XM_017009178.1:c.12139-21C>A	XP_016864667.1:n.12139-21C>A
XM_017009179.2:c.12139-21C>A	XP_016864668.1:n.12139-21C>A
XM_017009185.1:c.8323-21C>A	XP_016864674.1:n.8323-21C>A
XM_017009186.1:c.7876-21C>A	XP_016864675.1:n.7876-21C>A
XM_017009188.1:c.7213-21C>A	XP_016864677.1:n.7213-21C>A
XM_024454388.1:c.12139-21C>A	XP_024310156.1:n.12139-21C>A
XM_024454389.1:c.11728-21C>A	XP_024310157.1:n.11728-21C>A
NM_001369.3:c.13126-21C>A MANE Select	NP_001360.1:n.13126-21C>A