Canonical Allele Identifier: CA345384648

Gene: MTR

Linked Data

• MyVariant Identifiers: chr1:g.237048506A>C (hg19) ; chr1:g.236885206A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236885206A>C , CM000663.2:g.236885206A>C	GRCh38
NC_000001.10:g.237048506A>C , CM000663.1:g.237048506A>C	GRCh37
NC_000001.9:g.235115129A>C	NCBI36
NG_008959.1:g.94926A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000366577.10:c.2762A>C MANE Select	ENSP00000355536.5:p.Tyr921Ser
ENST00000535889.6:c.2609A>C	ENSP00000441845.1:p.Tyr870Ser
ENST00000650888.1:c.*1804A>C	ENSP00000498393.1:n.*1804A>C
ENST00000651455.1:c.*1506A>C	ENSP00000498963.1:n.*1506A>C
ENST00000674797.2:c.2414A>C	ENSP00000502299.2:p.Tyr805Ser
ENST00000679569.1:n.3076A>C
ENST00000679842.1:c.2573A>C	ENSP00000506109.1:p.Tyr858Ser
ENST00000680454.1:n.3206A>C
ENST00000681102.1:c.2582A>C	ENSP00000505600.1:p.Tyr861Ser
ENST00000681177.1:c.2324A>C	ENSP00000506327.1:p.Tyr775Ser
ENST00000681937.1:n.2956A>C
ENST00000366576.3:c.1424A>C	ENSP00000355535.3:p.Tyr475Ser
ENST00000366577.9:c.2762A>C	ENSP00000355536.5:p.Tyr921Ser
ENST00000535889.5:c.2609A>C	ENSP00000441845.1:p.Tyr870Ser
NM_000254.2:c.2762A>C	NP_000245.2:p.Tyr921Ser
NM_001291939.1:c.2609A>C	NP_001278868.1:p.Tyr870Ser
NM_001291940.1:c.1541A>C	NP_001278869.1:p.Tyr514Ser
XM_005273141.3:c.2759A>C	XP_005273198.1:p.Tyr920Ser
XM_006711769.2:c.2762A>C	XP_006711832.1:p.Tyr921Ser
XM_006711770.1:c.1826A>C	XP_006711833.1:p.Tyr609Ser
XM_011544193.1:c.2573A>C	XP_011542495.1:p.Tyr858Ser
XM_011544194.1:c.2930A>C	XP_011542496.1:p.Tyr977Ser
XM_005273141.5:c.2759A>C	XP_005273198.1:p.Tyr920Ser
XM_006711770.3:c.1826A>C	XP_006711833.1:p.Tyr609Ser
XM_011544194.3:c.2930A>C	XP_011542496.1:p.Tyr977Ser
XM_017001329.2:c.2777A>C	XP_016856818.1:p.Tyr926Ser
XM_017001330.2:c.2741A>C	XP_016856819.1:p.Tyr914Ser
NM_001291940.2:c.1541A>C	NP_001278869.1:p.Tyr514Ser
NM_000254.3:c.2762A>C MANE Select	NP_000245.2:p.Tyr921Ser