Canonical Allele Identifier: CA3201858

Gene: DNAH5

Linked Data

• dbSNP Id: rs373620771
• ExAC: 5:13735214 G / A
• gnomAD v2: 5-13735214-G-A
• gnomAD v3: 5-13735105-G-A
• gnomAD v4: 5-13735105-G-A
• MyVariant Identifiers: chr5:g.13735214G>A (hg19) ; chr5:g.13735105G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13735105G>A , CM000667.2:g.13735105G>A	GRCh38
NC_000005.9:g.13735214G>A , CM000667.1:g.13735214G>A	GRCh37
NC_000005.8:g.13788214G>A	NCBI36
NG_013081.1:g.214376C>T
NG_013081.2:g.214376C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.11761+26C>T MANE Select	ENSP00000265104.4:n.11761+26C>T
ENST00000681290.1:c.11716+26C>T	ENSP00000505288.1:n.11716+26C>T
ENST00000265104.4:c.11761+26C>T	ENSP00000265104.4:n.11761+26C>T
NM_001369.2:c.11761+26C>T	NP_001360.1:n.11761+26C>T
XM_005248262.2:c.11716+26C>T	XP_005248319.1:n.11716+26C>T
XM_005248262.3:c.11869+26C>T	XP_005248319.2:n.11869+26C>T
XM_017009177.1:c.11869+26C>T	XP_016864666.1:n.11869+26C>T
XM_017009178.1:c.10774+26C>T	XP_016864667.1:n.10774+26C>T
XM_017009179.2:c.10774+26C>T	XP_016864668.1:n.10774+26C>T
XM_017009180.1:c.11869+26C>T	XP_016864669.1:n.11869+26C>T
XM_017009181.1:c.11869+26C>T	XP_016864670.1:n.11869+26C>T
XM_017009185.1:c.6958+26C>T	XP_016864674.1:n.6958+26C>T
XM_017009186.1:c.6511+26C>T	XP_016864675.1:n.6511+26C>T
XM_017009188.1:c.5848+26C>T	XP_016864677.1:n.5848+26C>T
XM_024454388.1:c.10774+26C>T	XP_024310156.1:n.10774+26C>T
XM_024454389.1:c.10363+26C>T	XP_024310157.1:n.10363+26C>T
NM_001369.3:c.11761+26C>T MANE Select	NP_001360.1:n.11761+26C>T