Canonical Allele Identifier: CA824259403

Gene: LHFPL5

Linked Data

• dbSNP Id: rs1193008021
• MyVariant Identifiers: chr6:g.35791244_35791245insCTCT (hg19) ; chr6:g.35823467_35823468insCTCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35823468_35823469insTCTC , CM000668.2:g.35823468_35823469insTCTC	GRCh38
NC_000006.11:g.35791245_35791246insTCTC , CM000668.1:g.35791245_35791246insTCTC	GRCh37
NC_000006.10:g.35899223_35899224insTCTC	NCBI36
NG_012184.1:g.23175_23176insTCTC
NG_012184.2:g.23175_23176insTCTC
NG_012184.3:g.31263_31264insTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360215.3:c.*503_*504insTCTC MANE Select	ENSP00000353346.1:n.*503_*504insTCTC
ENST00000496656.2:n.578+3648_578+3649insTCTC
ENST00000651132.1:c.*503_*504insTCTC	ENSP00000498322.1:n.*503_*504insTCTC
ENST00000651676.1:c.*16+4005_*16+4006insTCTC	ENSP00000498699.1:n.*16+4005_*16+4006insTCTC
ENST00000651994.1:c.*583_*584insTCTC	ENSP00000498310.1:n.*583_*584insTCTC
ENST00000652718.1:c.508+4005_508+4006insTCTC	ENSP00000498866.1:n.508+4005_508+4006insTCTC
ENST00000360215.2:c.*503_*504insTCTC	ENSP00000353346.1:n.*503_*504insTCTC
ENST00000496656.1:n.812+3648_812+3649insTCTC
NM_182548.3:c.*503_*504insTCTC	NP_872354.1:n.*503_*504insTCTC
NM_182548.4:c.*503_*504insTCTC MANE Select	NP_872354.1:n.*503_*504insTCTC