Canonical Allele Identifier: CA1394947073

Gene: LSAMP

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.116021872A= , CM000665.2:g.116021872A=	GRCh38
NC_000003.11:g.115740719A= , CM000665.1:g.115740719A=	GRCh37
NC_000003.10:g.117223409A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490035.7:c.389-2232T= MANE Select	ENSP00000419000.1:n.389-2232T=
ENST00000333617.8:c.341-2232T=	ENSP00000328455.4:n.341-2232T=
ENST00000474851.1:c.491-2232T=	ENSP00000418506.1:n.491-2232T=
ENST00000490035.6:c.389-2232T=	ENSP00000419000.1:n.389-2232T=
ENST00000498645.1:n.98-2232T=
ENST00000539563.5:c.239-2232T=	ENSP00000443429.2:n.239-2232T=
NM_002338.3:c.389-2232T=	NP_002329.2:n.389-2232T=
XM_005247454.2:c.389-2232T=	XP_005247511.1:n.389-2232T=
XM_011512838.1:c.389-2232T=	XP_011511140.1:n.389-2232T=
XM_011512839.1:c.389-2232T=	XP_011511141.1:n.389-2232T=
XM_011512840.1:c.389-2232T=	XP_011511142.1:n.389-2232T=
XR_924139.1:n.900-2232T=
NM_001318915.1:c.389-2232T=	NP_001305844.1:n.389-2232T=
NM_002338.4:c.389-2232T=	NP_002329.2:n.389-2232T=
XM_011512840.3:c.389-2232T=	XP_011511142.1:n.389-2232T=
XM_017006383.2:c.389-2232T=	XP_016861872.1:n.389-2232T=
XM_024453520.1:c.98-2232T=	XP_024309288.1:n.98-2232T=
XM_024453521.1:c.98-2232T=	XP_024309289.1:n.98-2232T=
NM_002338.5:c.389-2232T= MANE Select	NP_002329.2:n.389-2232T=
NM_001318915.2:c.389-2232T=	NP_001305844.1:n.389-2232T=