Canonical Allele Identifier: CA1734199160

Gene: IMMP2L

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.110700918T= , CM000669.2:g.110700918T=	GRCh38
NC_000007.13:g.110340974T= , CM000669.1:g.110340974T=	GRCh37
NC_000007.12:g.110128210T=	NCBI36
NG_030016.1:g.866600A=
NG_030016.2:g.866600A=

Transcript Alleles

HGVS	Amino-acid Change
NM_032549.4:c.409-37197A= MANE Select	NP_115938.1:n.409-37197A=
ENST00000405709.7:c.409-37197A= MANE Select	ENSP00000384966.2:n.409-37197A=
NM_001244606.1:c.409-37197A=	NP_001231535.1:n.409-37197A=
NM_001244606.2:c.409-37197A=	NP_001231535.1:n.409-37197A=
NM_001350959.1:c.409-37197A=	NP_001337888.1:n.409-37197A=
NM_001350959.2:c.409-37197A=	NP_001337888.1:n.409-37197A=
NM_001350960.1:c.409-37197A=	NP_001337889.1:n.409-37197A=
NM_001350960.2:c.409-37197A=	NP_001337889.1:n.409-37197A=
NM_001350961.1:c.493-37197A=	NP_001337890.1:n.493-37197A=
NM_001350961.2:c.493-37197A=	NP_001337890.1:n.493-37197A=
NM_001350963.1:c.306-37197A=	NP_001337892.1:n.306-37197A=
NM_001350963.2:c.306-37197A=	NP_001337892.1:n.306-37197A=
NM_032549.3:c.409-37197A=	NP_115938.1:n.409-37197A=
ENST00000331762.7:c.409-37197A=	ENSP00000329553.3:n.409-37197A=
ENST00000405709.6:c.409-37197A=	ENSP00000384966.2:n.409-37197A=
ENST00000450877.5:c.355-37197A=	ENSP00000402824.1:n.355-37197A=
ENST00000452895.5:c.409-37197A=	ENSP00000399353.1:n.409-37197A=
ENST00000487733.5:n.67-37197A=
ENST00000489381.1:n.247-35906A=
XM_005250630.3:c.409-37197A=	XP_005250687.1:n.409-37197A=
XM_011516605.1:c.493-37197A=	XP_011514907.1:n.493-37197A=
XM_011516609.1:c.390-37197A=	XP_011514911.1:n.390-37197A=
XM_011516609.2:c.390-37197A=	XP_011514911.1:n.390-37197A=
XM_011516613.1:c.306-37197A=	XP_011514915.1:n.306-37197A=
XM_024446956.1:c.286-37197A=	XP_024302724.1:n.286-37197A=