Canonical Allele Identifier: CA502685958

Gene: LPIN2 CHORDC1P4

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.2946293C>A , CM000680.2:g.2946293C>A	GRCh38
NC_000018.9:g.2946291C>A , CM000680.1:g.2946291C>A	GRCh37
NC_000018.8:g.2936291C>A	NCBI36
NG_007507.1:g.70655G>T , LRG_174:g.70655G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001375808.2:c.590+4762G>T (LPIN2) MANE Select	NP_001362737.1:n.590+4762G>T
ENST00000677752.1:c.590+4762G>T (LPIN2) MANE Select	ENSP00000504857.1:n.590+4762G>T
NM_001375808.1:c.590+4762G>T (LPIN2)	NP_001362737.1:n.590+4762G>T
NM_001375809.1:c.590+4762G>T (LPIN2)	NP_001362738.1:n.590+4762G>T
NM_014646.2:c.590+4762G>T , LRG_174t1:c.590+4762G>T (LPIN2)	NP_055461.1:n.590+4762G>T
NR_026659.1:n.331G>T (CHORDC1P4)
ENST00000261596.8:c.590+4762G>T (LPIN2)	ENSP00000261596.4:n.590+4762G>T
ENST00000261596.9:c.590+4762G>T (LPIN2)	ENSP00000261596.4:n.590+4762G>T
ENST00000581139.1:n.598G>T (CHORDC1P4)
ENST00000582850.1:n.242G>T (CHORDC1P4)
ENST00000584294.1:c.590+4762G>T (LPIN2)	ENSP00000463026.1:n.590+4762G>T
ENST00000697039.1:c.590+4762G>T (LPIN2)	ENSP00000513061.1:n.590+4762G>T
ENST00000697040.1:c.590+4762G>T (LPIN2)	ENSP00000513062.1:n.590+4762G>T
ENST00000697042.1:c.590+4762G>T (LPIN2)	ENSP00000513064.1:n.590+4762G>T
XM_005258177.3:c.701+4762G>T (LPIN2)	XP_005258234.1:n.701+4762G>T
XM_005258177.4:c.701+4762G>T (LPIN2)	XP_005258234.1:n.701+4762G>T
XM_005258178.2:c.590+4762G>T (LPIN2)	XP_005258235.1:n.590+4762G>T
XM_005258178.3:c.590+4762G>T (LPIN2)	XP_005258235.1:n.590+4762G>T
XM_005258179.3:c.590+4762G>T (LPIN2)	XP_005258236.1:n.590+4762G>T
XM_005258179.5:c.590+4762G>T (LPIN2)	XP_005258236.1:n.590+4762G>T
XM_017026098.1:c.590+4762G>T (LPIN2)	XP_016881587.1:n.590+4762G>T
XM_017026099.1:c.590+4762G>T (LPIN2)	XP_016881588.1:n.590+4762G>T
XR_935074.1:n.719+4762G>T (LPIN2)
XR_935074.2:n.764+4762G>T (LPIN2)