Canonical Allele Identifier: CA359207213

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13717512C>G (hg19) ; chr5:g.13717403C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13717403C>G , CM000667.2:g.13717403C>G	GRCh38
NC_000005.9:g.13717512C>G , CM000667.1:g.13717512C>G	GRCh37
NC_000005.8:g.13770512C>G	NCBI36
NG_013081.1:g.232078G>C
NG_013081.2:g.232078G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.12617G>C MANE Select	ENSP00000265104.4:p.Trp4206Ser
ENST00000681290.1:c.12572G>C	ENSP00000505288.1:p.Trp4191Ser
ENST00000265104.4:c.12617G>C	ENSP00000265104.4:p.Trp4206Ser
NM_001369.2:c.12617G>C	NP_001360.1:p.Trp4206Ser
XM_005248262.2:c.12572G>C	XP_005248319.1:p.Trp4191Ser
XM_005248262.3:c.12725G>C	XP_005248319.2:p.Trp4242Ser
XM_017009177.1:c.12725G>C	XP_016864666.1:p.Trp4242Ser
XM_017009178.1:c.11630G>C	XP_016864667.1:p.Trp3877Ser
XM_017009179.2:c.11630G>C	XP_016864668.1:p.Trp3877Ser
XM_017009180.1:c.12725G>C	XP_016864669.1:p.Trp4242Ser
XM_017009185.1:c.7814G>C	XP_016864674.1:p.Trp2605Ser
XM_017009186.1:c.7367G>C	XP_016864675.1:p.Trp2456Ser
XM_017009188.1:c.6704G>C	XP_016864677.1:p.Trp2235Ser
XM_024454388.1:c.11630G>C	XP_024310156.1:p.Trp3877Ser
XM_024454389.1:c.11219G>C	XP_024310157.1:p.Trp3740Ser
NM_001369.3:c.12617G>C MANE Select	NP_001360.1:p.Trp4206Ser