Canonical Allele Identifier: CA1734264087

Gene: IMMP2L

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.110827193C= , CM000669.2:g.110827193C=	GRCh38
NC_000007.13:g.110467249C= , CM000669.1:g.110467249C=	GRCh37
NC_000007.12:g.110254485C=	NCBI36
NG_030016.1:g.740325G=
NG_030016.2:g.740325G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405709.7:c.408+59400G= MANE Select	ENSP00000384966.2:n.408+59400G=
ENST00000331762.7:c.408+59400G=	ENSP00000329553.3:n.408+59400G=
ENST00000405709.6:c.408+59400G=	ENSP00000384966.2:n.408+59400G=
ENST00000450877.5:c.354+59400G=	ENSP00000402824.1:n.354+59400G=
ENST00000452895.5:c.408+59400G=	ENSP00000399353.1:n.408+59400G=
ENST00000487733.5:n.66+136307G=
ENST00000489381.1:n.246+136307G=
NM_001244606.1:c.408+59400G=	NP_001231535.1:n.408+59400G=
NM_032549.3:c.408+59400G=	NP_115938.1:n.408+59400G=
XM_005250630.3:c.408+59400G=	XP_005250687.1:n.408+59400G=
XM_011516605.1:c.492+59400G=	XP_011514907.1:n.492+59400G=
XM_011516608.1:c.492+59400G=	XP_011514910.1:n.492+59400G=
XM_011516609.1:c.389+136307G=	XP_011514911.1:n.389+136307G=
XM_011516613.1:c.305+136307G=	XP_011514915.1:n.305+136307G=
NM_001350959.1:c.408+59400G=	NP_001337888.1:n.408+59400G=
NM_001350960.1:c.408+59400G=	NP_001337889.1:n.408+59400G=
NM_001350961.1:c.492+59400G=	NP_001337890.1:n.492+59400G=
NM_001350963.1:c.305+136307G=	NP_001337892.1:n.305+136307G=
XM_011516608.2:c.492+59400G=	XP_011514910.1:n.492+59400G=
XM_011516609.2:c.389+136307G=	XP_011514911.1:n.389+136307G=
XM_017012704.1:c.492+59400G=	XP_016868193.1:n.492+59400G=
XM_024446956.1:c.285+59400G=	XP_024302724.1:n.285+59400G=
NM_001244606.2:c.408+59400G=	NP_001231535.1:n.408+59400G=
NM_001350959.2:c.408+59400G=	NP_001337888.1:n.408+59400G=
NM_001350960.2:c.408+59400G=	NP_001337889.1:n.408+59400G=
NM_001350961.2:c.492+59400G=	NP_001337890.1:n.492+59400G=
NM_001350963.2:c.305+136307G=	NP_001337892.1:n.305+136307G=
NM_032549.4:c.408+59400G= MANE Select	NP_115938.1:n.408+59400G=