Canonical Allele Identifier: CA374932403

Gene: LRSAM1

Linked Data

• MyVariant Identifiers: chr9:g.130248072A>C (hg19) ; chr9:g.127485793A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127485793A>C , CM000671.2:g.127485793A>C	GRCh38
NC_000009.11:g.130248072A>C , CM000671.1:g.130248072A>C	GRCh37
NC_000009.10:g.129287893A>C	NCBI36
NG_032008.1:g.39308A>C , LRG_373:g.39308A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.1217A>C MANE Select	ENSP00000300417.6:p.Tyr406Ser
ENST00000472068.2:c.*940A>C	ENSP00000501555.1:n.*940A>C
ENST00000498513.6:c.470A>C	ENSP00000501637.1:p.Tyr157Ser
ENST00000674511.1:n.1092A>C
ENST00000674516.1:c.1217A>C	ENSP00000502441.1:p.Tyr406Ser
ENST00000674621.1:n.1123A>C
ENST00000674771.1:c.1217A>C	ENSP00000502627.1:p.Tyr406Ser
ENST00000674784.1:c.*376A>C	ENSP00000501837.1:n.*376A>C
ENST00000674970.1:c.*991A>C	ENSP00000502493.1:n.*991A>C
ENST00000675012.1:n.1097A>C
ENST00000675141.1:c.1217A>C	ENSP00000502420.1:p.Tyr406Ser
ENST00000675198.1:n.1119A>C
ENST00000675213.1:c.1172A>C	ENSP00000502218.1:p.Tyr391Ser
ENST00000675224.1:c.1217A>C	ENSP00000501869.1:p.Tyr406Ser
ENST00000675253.1:c.1217A>C	ENSP00000502557.1:p.Tyr406Ser
ENST00000675445.1:c.*889A>C	ENSP00000502253.1:n.*889A>C
ENST00000675448.1:c.1217A>C	ENSP00000502167.1:p.Tyr406Ser
ENST00000675521.1:n.1069A>C
ENST00000675572.1:c.1217A>C	ENSP00000501598.1:p.Tyr406Ser
ENST00000675641.1:c.1217A>C	ENSP00000501845.1:p.Tyr406Ser
ENST00000675657.1:c.1217A>C	ENSP00000502002.1:p.Tyr406Ser
ENST00000675662.1:n.1082+28A>C
ENST00000675789.1:c.1217A>C	ENSP00000501954.1:p.Tyr406Ser
ENST00000675883.1:c.1217A>C	ENSP00000501592.1:p.Tyr406Ser
ENST00000675945.1:c.1217A>C	ENSP00000501835.1:p.Tyr406Ser
ENST00000676014.1:c.1160A>C	ENSP00000502058.1:p.Tyr387Ser
ENST00000676035.1:n.978A>C
ENST00000676106.1:n.1022A>C
ENST00000676137.1:n.1108A>C
ENST00000676170.1:c.1298A>C	ENSP00000502177.1:p.Tyr433Ser
ENST00000676318.1:c.1217A>C	ENSP00000502300.1:p.Tyr406Ser
ENST00000676336.1:c.995A>C	ENSP00000502686.1:p.Tyr332Ser
ENST00000676349.1:c.*986A>C	ENSP00000502155.1:n.*986A>C
ENST00000676399.1:n.1115A>C
ENST00000676409.1:n.1096A>C
ENST00000300417.10:c.1217A>C	ENSP00000300417.6:p.Tyr406Ser
ENST00000323301.8:c.1217A>C	ENSP00000322937.4:p.Tyr406Ser
ENST00000373322.1:c.1217A>C	ENSP00000362419.1:p.Tyr406Ser
ENST00000373324.8:c.1217A>C	ENSP00000362421.4:p.Tyr406Ser
ENST00000472068.1:n.204A>C
ENST00000483302.5:n.434A>C
ENST00000498513.5:n.470A>C
NM_001005373.3:c.1217A>C	NP_001005373.1:p.Tyr406Ser
NM_001005374.3:c.1217A>C	NP_001005374.1:p.Tyr406Ser
NM_001190723.2:c.1217A>C	NP_001177652.1:p.Tyr406Ser
NM_138361.5:c.1217A>C , LRG_373t1:c.1217A>C	NP_612370.3:p.Tyr406Ser
XM_006717316.2:c.1217A>C	XP_006717379.1:p.Tyr406Ser
XR_929874.1:n.1589A>C
XM_006717316.4:c.1217A>C	XP_006717379.1:p.Tyr406Ser
XM_017015283.1:c.1217A>C	XP_016870772.1:p.Tyr406Ser
XM_017015284.2:c.428A>C	XP_016870773.1:p.Tyr143Ser
XR_001746415.2:n.1571A>C
XR_929874.3:n.1571A>C
NM_001190723.3:c.1217A>C	NP_001177652.1:p.Tyr406Ser
NM_001005373.4:c.1217A>C MANE Select	NP_001005373.1:p.Tyr406Ser
NM_001005374.4:c.1217A>C	NP_001005374.1:p.Tyr406Ser
NM_001384142.1:c.1217A>C	NP_001371071.1:p.Tyr406Ser
NM_001384143.1:c.1217A>C	NP_001371072.1:p.Tyr406Ser
NM_001384144.1:c.428A>C	NP_001371073.1:p.Tyr143Ser
NR_168891.1:n.1565A>C
NR_168892.1:n.1565A>C