Canonical Allele Identifier: CA381936316

Gene: MYO7A

Linked Data

• gnomAD v4: 11-77211326-G-T
• MyVariant Identifiers: chr11:g.76922371G>T (hg19) ; chr11:g.77211326G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77211326G>T , CM000673.2:g.77211326G>T	GRCh38
NC_000011.9:g.76922371G>T , CM000673.1:g.76922371G>T	GRCh37
NC_000011.8:g.76600019G>T	NCBI36
NG_009086.1:g.88062G>T
NG_009086.2:g.88081G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.6226G>T MANE Select	ENSP00000386331.3:p.Asp2076Tyr
ENST00000670577.1:c.4027G>T
ENST00000409619.6:c.6079G>T	ENSP00000386635.2:p.Asp2027Tyr
ENST00000409709.7:c.6226G>T	ENSP00000386331.3:p.Asp2076Tyr
ENST00000458169.2:c.3652G>T	ENSP00000417017.2:p.Asp1218Tyr
ENST00000458637.6:c.6112G>T	ENSP00000392185.2:p.Asp2038Tyr
ENST00000481328.7:n.3762G>T
ENST00000526863.2:n.25+415G>T
ENST00000605744.1:n.1693G>T
NM_000260.3:c.6226G>T	NP_000251.3:p.Asp2076Tyr
NM_001127180.1:c.6112G>T	NP_001120652.1:p.Asp2038Tyr
XM_005274012.2:c.6109G>T	XP_005274069.1:p.Asp2037Tyr
XM_006718558.2:c.6217G>T	XP_006718621.1:p.Asp2073Tyr
XM_006718559.2:c.6112G>T	XP_006718622.1:p.Asp2038Tyr
XM_006718560.2:c.6109G>T	XP_006718623.1:p.Asp2037Tyr
XM_006718561.2:c.6112G>T	XP_006718624.1:p.Asp2038Tyr
XM_011545044.1:c.6226G>T	XP_011543346.1:p.Asp2076Tyr
XM_011545045.1:c.6220G>T	XP_011543347.1:p.Asp2074Tyr
XM_011545046.1:c.6193G>T	XP_011543348.1:p.Asp2065Tyr
XM_011545047.1:c.6130G>T	XP_011543349.1:p.Asp2044Tyr
XM_011545048.1:c.6001G>T	XP_011543350.1:p.Asp2001Tyr
XM_011545049.1:c.5989G>T	XP_011543351.1:p.Asp1997Tyr
XM_011545050.1:c.5962G>T	XP_011543352.1:p.Asp1988Tyr
XM_011545051.1:c.6226G>T	XP_011543353.1:p.Asp2076Tyr
XR_949938.1:n.6546G>T
XR_949941.1:n.6520G>T
XM_011545044.2:c.6226G>T	XP_011543346.1:p.Asp2076Tyr
XM_011545046.2:c.6316G>T	XP_011543348.2:p.Asp2106Tyr
XM_011545050.2:c.5962G>T	XP_011543352.1:p.Asp1988Tyr
XM_017017778.1:c.6310G>T	XP_016873267.1:p.Asp2104Tyr
XM_017017779.1:c.6307G>T	XP_016873268.1:p.Asp2103Tyr
XM_017017780.1:c.6316G>T	XP_016873269.1:p.Asp2106Tyr
XM_017017781.1:c.6220G>T	XP_016873270.1:p.Asp2074Tyr
XM_017017782.1:c.6202G>T	XP_016873271.1:p.Asp2068Tyr
XM_017017783.1:c.6199G>T	XP_016873272.1:p.Asp2067Tyr
XM_017017784.1:c.6199G>T	XP_016873273.1:p.Asp2067Tyr
XM_017017785.1:c.6079G>T	XP_016873274.1:p.Asp2027Tyr
XM_017017786.1:c.6316G>T	XP_016873275.1:p.Asp2106Tyr
XM_017017788.1:c.6202G>T	XP_016873277.1:p.Asp2068Tyr
XR_001747885.1:n.6305G>T
XR_001747887.1:n.6291G>T
NM_000260.4:c.6226G>T MANE Select	NP_000251.3:p.Asp2076Tyr
NM_001127180.2:c.6112G>T	NP_001120652.1:p.Asp2038Tyr
NM_001369365.1:c.6079G>T	NP_001356294.1:p.Asp2027Tyr