Canonical Allele Identifier: CA359209192

Gene: DNAH5

Linked Data

• dbSNP Id: rs948730317
• gnomAD v3: 5-13776612-T-G
• gnomAD v4: 5-13776612-T-G
• MyVariant Identifiers: chr5:g.13776721T>G (hg19) ; chr5:g.13776612T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13776612T>G , CM000667.2:g.13776612T>G	GRCh38
NC_000005.9:g.13776721T>G , CM000667.1:g.13776721T>G	GRCh37
NC_000005.8:g.13829721T>G	NCBI36
NG_013081.1:g.172869A>C
NG_013081.2:g.172869A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9200A>C MANE Select	ENSP00000265104.4:p.Asn3067Thr
ENST00000681290.1:c.9155A>C	ENSP00000505288.1:p.Asn3052Thr
ENST00000265104.4:c.9200A>C	ENSP00000265104.4:p.Asn3067Thr
NM_001369.2:c.9200A>C	NP_001360.1:p.Asn3067Thr
XM_005248262.2:c.9155A>C	XP_005248319.1:p.Asn3052Thr
XM_005248262.3:c.9308A>C	XP_005248319.2:p.Asn3103Thr
XM_017009177.1:c.9308A>C	XP_016864666.1:p.Asn3103Thr
XM_017009178.1:c.8213A>C	XP_016864667.1:p.Asn2738Thr
XM_017009179.2:c.8213A>C	XP_016864668.1:p.Asn2738Thr
XM_017009180.1:c.9308A>C	XP_016864669.1:p.Asn3103Thr
XM_017009181.1:c.9308A>C	XP_016864670.1:p.Asn3103Thr
XM_017009182.1:c.9308A>C	XP_016864671.1:p.Asn3103Thr
XM_017009183.1:c.9308A>C	XP_016864672.1:p.Asn3103Thr
XM_017009185.1:c.4397A>C	XP_016864674.1:p.Asn1466Thr
XM_017009186.1:c.3950A>C	XP_016864675.1:p.Asn1317Thr
XM_017009188.1:c.3287A>C	XP_016864677.1:p.Asn1096Thr
XM_024454388.1:c.8213A>C	XP_024310156.1:p.Asn2738Thr
XM_024454389.1:c.7802A>C	XP_024310157.1:p.Asn2601Thr
NM_001369.3:c.9200A>C MANE Select	NP_001360.1:p.Asn3067Thr