Canonical Allele Identifier: CA913074962

Gene: MPL

Linked Data

• MyVariant Identifiers: chr1:g.43814837_43814838del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43349166_43349167del , CM000663.2:g.43349166_43349167del	GRCh38
NC_000001.10:g.43814837_43814838del , CM000663.1:g.43814837_43814838del	GRCh37
NC_000001.9:g.43587424_43587425del	NCBI36
NG_007525.1:g.16363_16364del , LRG_510:g.16363_16364del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372470.9:c.1469-97_1469-96del MANE Select	ENSP00000361548.3:n.1469-97_1469-96del
ENST00000413998.7:c.1448-97_1448-96del	ENSP00000414004.3:n.1448-97_1448-96del
ENST00000638732.1:n.1469-97_1469-96del
ENST00000372470.7:c.1469-97_1469-96del	ENSP00000361548.3:n.1469-97_1469-96del
ENST00000413998.6:c.1469-97_1469-96del	ENSP00000414004.2:n.1469-97_1469-96del
ENST00000612993.1:c.1469-97_1469-96del	ENSP00000480273.1:n.1469-97_1469-96del
NM_005373.2:c.1469-97_1469-96del , LRG_510t1:c.1469-97_1469-96del	NP_005364.1:n.1469-97_1469-96del
XM_011541478.1:c.1448-97_1448-96del	XP_011539780.1:n.1448-97_1448-96del
XM_017001320.1:c.1640-97_1640-96del	XP_016856809.1:n.1640-97_1640-96del
NM_005373.3:c.1469-97_1469-96del MANE Select	NP_005364.1:n.1469-97_1469-96del