Canonical Allele Identifier: CA884339624

Gene: MUC16

Linked Data

• dbSNP Id: rs1559168
• MyVariant Identifiers: chr19:g.8992420A>C (hg19) ; chr19:g.8881744A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8881744A>C , CM000681.2:g.8881744A>C	GRCh38
NC_000019.9:g.8992420A>C , CM000681.1:g.8992420A>C	GRCh37
NC_000019.8:g.8853420A>C	NCBI36
NG_055257.1:g.133647T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000710609.1:c.41872+587T>G	ENSP00000518375.1:n.41872+587T>G
ENST00000710610.1:c.32578+587T>G	ENSP00000518376.1:n.32578+587T>G
ENST00000711672.1:c.41938+587T>G	ENSP00000518832.1:n.41938+587T>G
ENST00000397910.8:c.41752+587T>G	ENSP00000381008.2:n.41752+587T>G
ENST00000596768.5:c.1610+587T>G
ENST00000599436.1:c.2271+587T>G
ENST00000601404.5:c.2205+587T>G
NM_024690.2:c.41752+587T>G	NP_078966.2:n.41752+587T>G
XM_017027486.1:c.41002+587T>G	XP_016882975.1:n.41002+587T>G
XM_017027487.1:c.40936+587T>G	XP_016882976.1:n.40936+587T>G
XM_017027488.1:c.41002+587T>G	XP_016882977.1:n.41002+587T>G
XM_017027489.1:c.40882+587T>G	XP_016882978.1:n.40882+587T>G
XM_017027490.1:c.40537+587T>G	XP_016882979.1:n.40537+587T>G
XM_017027491.1:c.40537+587T>G	XP_016882980.1:n.40537+587T>G
XM_017027492.1:c.40534+587T>G	XP_016882981.1:n.40534+587T>G
XM_017027493.1:c.40534+587T>G	XP_016882982.1:n.40534+587T>G
XM_017027494.1:c.40534+587T>G	XP_016882983.1:n.40534+587T>G
XM_017027495.1:c.40534+587T>G	XP_016882984.1:n.40534+587T>G
XM_017027499.1:c.31789+587T>G	XP_016882988.1:n.31789+587T>G
XM_017027500.1:c.31708+587T>G	XP_016882989.1:n.31708+587T>G
XM_017027501.1:c.3676+587T>G	XP_016882990.1:n.3676+587T>G